PRODUCT RECALL | Men’s Weightloss Drug due to Undeclared Drugs

Men’s weight loss products Recalled for Undeclared Drugs

Posted on August 9, 2015 by

Blue Square Market Inc. of North Huntingdon, PA, is recalling “Kaboom Actions Strip 12 Pack” and LiDa DaiDaiHua to the user level after FDA analysis revealed the products contain undeclared active pharmaceutical ingredients. Kaboom was found to contain sulfoaildenafil and LiDa DaiDaiHua was found to contain sibutramine and phenolphthalein.

Kaboom Actions Strips are marketed for men’s vitality and LiDa DaiDaiHua is marketed for weightloss. Kaboom Actions Strips was purchased from the manufacturer Nutrology USA, LLC. Kaboom Action Strips comes in packages of 12 strips in a black box with a picture of the strip on the front of the box and a stamped expiration date of 9/17 on the box. LiDa DaiDaiHua was purchased from the manufacturer Green Cross Store. LiDa DaiDaiHua comes in a light green and grey box with a picture of a woman on the front, with a stamped expiration date of 1/17 on the bottom.

Blue Square Market’s online store, was one of many that sold these retail products. Blue Square Market is neither the manufacturer nor the distributor of the product, only a retailer. Blue Square Market has pulled all of Kaboom Actions Strip 12 Pack and Lida DaiDaiHua from its online store,, and will no longer carry this product line.

Blue Square Market is notifying its customers by letter and is arranging for return and refund of all recalled products. Consumers who have purchased Kaboom Actions Strip 12 Pack from March 20, 2015 to July 7, 2015 with expiration date of 9/17 or Lida DaiDaiHua from Feb 23, 2015 to May 7, 2015 with expiration date of 1/17should immediately discontinue use and return them to Blue Square Market, Inc. for a full refund.

Consumers with questions regarding this recall can contact Blue Square market by phone at 1-877-919-9992 Monday – Friday from 9am to 4:30pm EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

© 2015 US Food Safety Corporation. No copyright claim is made for portions of this blog and linked items that are works of the United States Government, state governments or third parties.


2015 The NW Fire Blog

PRODUCT RECALL: Slingslot by Barnett Outdoors due to Risk of Injury

The CPSC wants the public know a product recall by Barnett Outdoors LLC, of Tarpon Springs, Florida has issued a product recall for hunting and sports slingslots due to risk of injury.

Barnett Outdoors Black Widow Slingshot

#Image courtesy of

The recall is due to slingshot’s wrist strap can slip off the wrist brace when the slingshot’s pouch is pulled back which can result in the body of the slingshot snapping back and striking the user.

Barnett has received two reports of the wrist strap slipping off and the body of the sling striking the users in the face, with one consumer receiving bruises and the other suffering facial fractures.

Recalled slingshots have no X markings on the ends of the wrist wrap.

#Image Courtesy of

Approximately 88,000 in the US and 16,000 sold in Canada are affected.

The Manufacturer recommends consumers should immediately stop using the recalled slingshots and contact Barnett to receive a free replacement wrist strap.

Consumers can call Barnett Outdoors at (800) 234-4907, extension 2, from 9 a.m. to 5 p.m. ET Monday through Friday or online at and click on BLACK WIDOW RECALL for more information.

These products are reportedly sold from July 2014 to May 2015 for about $10.

  • A.C. Kerman
  • Archery Range
  • Archery Shoppe
  • Big Rock Sporting Goods
  • Bow Hunters Supply Store
  • Campco
  • Dicks Sporting Goods
  • Dunham’s
  • Florida Hardware Co.
  • Great Lakes Marine Products
  • Gun World & Sporting Goods
  • Paducah Shooters Supply
  • Slingshots USA
  • Walmart
  • Other archery, shooting and sports stores nationwide

[c] 2015 The NW Fire Blog

PRODUCT RECALL | Pill XL Portable Wireless Speakers by Apple | June 3, 2015

Cupertino CA

In partnership, Apple Inc and Beats Electronics LLC of Cupertino are recalling the Pill XL Portable Wireless Speakers [Beats Pill XL Speakers] by Apple manufactured in China due to the battery to overheat and cause a fire.

#ProductImages Courtesy of #CPSC:

apple appl2

There have been 8 incidents reported, with one consumer’s desk being burned and another receiving burns to his finger.

Affected Products

There are approximately 11,000 products in Canada and 222,000 in the United States.  Both the U.S. and Canada are working in conjunction with this product recall.


Contact Apple and ask for a refund.


Consumer Contact

Apple Inc. online at or or contact Apple Support toll-free at (800) 275-2273 anytime for more information.

[c] 2015 The NW Fire Blog

PRODUCT RECALL | Bikes & Fenders by Civia Cycles

Bloomington, MN | A product recall has been issued by Civia Cycles for approximately 1,000 Civia Bicycles and Aluminum Civia Fenders.  The recall states fender mounting bracket can break or bend posing a fall hazard to the rider.


One injury has been reported to the Civia in the bracket breaking causing the rider to fall.  The consumer suffered a cervical spine injury and resulting nerve damage.


The Tawainese manufactured product is imported by Civia Cyccles and branded as their own product.  Bikes and fenders were sold at independent bike dealers between April 2008 through March 2013.   Fenders were sold for $60 and bikes were sold between $1200-$4500.


Consumers can contact Civia Cycles at 877-311-7686 from 0800-1800 CT Monday – Friday or on their website at


PRODUCT RECALL | Children’s PJs by Smooth Industries due to Violation of Federal Flammability Standard

Children’s PJs are being recalled by Smooth Industries out of Oceanside, CA due to not meeting the Federal flammability Standard as set by the United States.  It’s manufacturer is based out of China.

Courtesy of

Courtesy of

Failing to meet the Standard is a risk of children getting burned.

Approximately 7,600 products are affected by this recall.

Courtesy of

Courtesy of

No incidents or injuries have been reported.

The recall states you can return the product for credit towards any Smooth Industries company product.

These products were sold for approximately $30 & $35 each at authorized motorcycle/cross stores from October 2012 through January 2015.


Smooth Industries can be reached Tuesday through Friday, 0900 – 1800 hours PDT at 1-844-216-2076 or by visiting their website at

This recall was released by the US Consumer Product Safety Commission.  More information can be found on their site at –>

Courtesy of

Courtesy of

[c] 2015 The NW Fire Blog

PRODUCT RECALL | Outdoor Patio Set Rockers due to Fall Hazard

Home Depot’s Bay branded Niles Park Collection patio sets SKU numbers #658479,  658480,  658485, 658486, 662696, 662688 and 100051056 are being recalled due to the chairs being a fall hazard.


Photo Courtesy |

Three incidents have been reported, resulting in no reports of injuries.

The chairs are manufactured by Guandong Shunde Baiming Industry of China and imported by Home Depot.

Approximately 25,000 units are affected by this recall.

Photo courtesy |

Photo courtesy |

If you have one of the above referenced units as under the SKU number found on the chair’s label, contact Dimensions at 1-800-598-6532 from 0900-1700 hours EST or you can go to their website at

[c] 2015 The NW Fire Blog

Product Recall | Residential Hydraulic Elevator by Coastal Carolina Elevators due to Crushing Hazard

Little River, SC | Coastal Carolina Elevators manufactrued by Cambridge Elevating of Canada is recalling approximately 240 of its elevators in response to a catastrophic brain injury to a 10-year-old boy from Baltimore, Md. and two other reports of incidents.

MANUFACTURER  | Cambridge Elevating 

PRODUCT NAME | Elmira Hydraulic residential hydraulic elevators

Coastal Carolina residential elevator

DISTRIBUTOR | Coastal Carolina Elevators LLC, formerly Seaside Elevator LLC.

SOLD AT  | Coastal Carolina Elevators through residential contractors and home builders, including DRHorton, in South Carolina from January 2006 through December 2009 for between $16,000 and $25,000.

CONSUMER CONTACT | Coastal Carolina Elevators collect at (843) 399-6545 from 9 a.m. to 5 p.m. ET Monday through Friday, or and click on the Recall tab at the top of the page (effective April 6, 2015).

THE HAZARD |   The elevator can operate while the gate door is open, posing a crushing hazard.

[c] 2015 The NW Fire Blog


Product Recall: Bernat Tizzy Yarn by Spinrite due to Entanglement Hazard

Washington NC | The Spinrite Yarns LP issued a recall for the Bernat Tizzy Yarn products due to an entanglement hazard and were soon pulled from the major craft stores, such as Michael’s, Joann’s and other retailers nationwide.

Bernat Tizzy Yarn


The U.S. Consumer Product Safety Commission received two reports of children being entangled from the unraveling or snagging of yarn blankets.  No reports of injuries reported at this time.


The recall includes all 11 colors of Bernat brand Tizzy Yarn. The yarn was sold as a ball or skein in a 3.5 ounce package with a paper sleeve. The green sleeve has a striped border with a photo of a baby in a knitted sweater and “Bernat” printed in all white capital letters and “Tizzy” printed in yellow and orange letters.   UPC codes included in the recall are printed under the barcode on the paper sleeve. Below is a full listing of the color numbers, color names and UPC codes included in the recall.

Color # Color Name UPC
24005 Marshmallow White 057355350380
24114 Playtime Denim 057355375970
24128 Blue Skies 057355350397
24230 Sweet Green Pea 057355350403
24305 Pixie Purple 057355350410
24412 Red Riding Hood 057355375987
24421 Posey Pink 057355350427
24611 Dandelion Yellow 057355350434
24627 Playtime 057355366336
24628 Creamsicle 057355350441
24711 Day Dream 057355355521


620,000 in the United States and 220,000 in Canada.


Jo-Ann Stores, Michaels and other craft retail stores nationwide and online at from April 2012 through February 2015 for between $4.50 and $5.


Bernat toll-free (844) 418-7973 from 8 a.m. to 5 p.m. ET Monday through Friday or online at and click on the “Voluntary Recall” button at the top of the page for more information.


Consumers should immediately stop using the yarn or finished yarn projects, keep them out of the reach of young children, and contact Bernat for a full refund.

[c] 2015 The NW Fire Blog


Product Recall | CreaMiser Refrigerated Creamer Dispensers due to Fire Hazards

Model 200

Broomfield CO | White Wave Foods formerly owned by CreaMiser Products of Phoenix Arizona products are currently under recall due to posing a Fire Hazard to Consumers.


This recall involves CreaMiser refrigerated coffee creamer dispensers for commercial use with model numbers 200, 210 and 400, digital thermometers and certain serial numbers. The plastic dispensers were sold in the following colors: black granite, gray granite and sand.

Models 200 and 210 have two creamer dispenser stations and model 400 has four creamer dispenser stations.  Model, serial number and “CreaMiser Products Corporation” are printed on a white sticker or metal name plate on the back of the dispensers.


Model numbers Serial numbers
200 CP200-02001 through CP200-05151
210 CP210-00001 through CP210-01925
400 CP400-02001 through CP400-05500

Approximately 5,600 units are affected in this recall.


The “Hazard” lists the product’s inside relay the creamer dispenser can overheat posing a fire hazard.

Model 210


Seven have been reported.  Two were from fires inside a repair facility and five had digital thermometers melted. No injuries reported.


Owners should immediately unplug the recalled creamer dispensers, remove them from service and contact CreaMiser for a free repair.


CreaMiser at (800) 905-3366 from 0730 – 1630 Hours Mountain Time, Monday through Friday or online and click on “CreaMiser Refrigerated Creamer Dispensers Recalled by WhiteWave” below the menu on the left side of the home page for more information.

Model 400


CPSC story & link |

[c] 2015 The NW Fire Blog






FDA Recall Alert: Dietary Supplements Recalled Due to Cause Overabundance of Rhizopus oryzae


FOR IMMEDIATE RELEASE — November 17, 2014 — Solgar, Inc., of Leonia, NJ, is voluntarily recalling ABC Dophilus® Powder. The recall was initiated, out of an abundance of caution, because the product was found to contain Rhizopus oryzae, which may cause Mucormycosis. This is a rare infection that may cause health problems to consumers, particularly pre-mature infants/infants, children, and those with weakened immune systems. Although, it may also occur (rarely) in people who are otherwise healthy. ABC Dophilus was used as part of the in-hospital course of treatment for a very preterm infant (<32 week gestation) who suffered from multiple complications, including intestinal mucormycosis, and died on October 11, 2014. Susceptible consumers should consult with their physician or health care provider if they have used this product.

Solgar is notifying consumers and customers not to consume this product

This product was distributed to: AL, AR, AZ, CA, CT, CO, FL, IA, IL, IN, MI, ME, MO, MA, NC, NE, NY, NJ, NV, OH, OK, PA, PR, UT, TN, TX, VT, KY, WI, WA, UK and Israel through pharmacy, retail stores, wholesale, internet, etc.

Description: Solgar ABC Dophilus® Powder NET Wt. 1.75 oz (50 g)
UPC Code: 0 33984 00010 0
Label: Solgar
Lot# 074024-01R1, 074024-01, 074024-02 Expiration
Date 7/31/15

Testing conducted by the Centers for Disease Control revealed the presence of Rhizopus oryzae in 1.75 oz (50 g) containers of Solgar ABC Dophilis Powder.

The distribution of the product has been suspended while FDA and the company continue to investigate the source of the problem.


Risk factors for developing Mucormycosis include: uncontrolled diabetes; cancer; organ transplant; neutropenia (low white blood cells); skin trauma (cuts, scrapes, punctures, or burns). Susceptible consumers should consult with their physician or health care provider.

Consumers who have purchased Solgar ABC Dophilus® Powder are urged not to consume the product and should return it to the place of purchase for a full refund. Consumers with questions may contact the company at 888-534-6370, Monday-Friday, 9AM-7PM ET.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:

Complete and submit the report Online:

Download form  []  or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.


2014 The NW Fire Blog