Wingman35 Crossing Catheter Recall [US]

US/Silver Spring: ReFlow Medical recalls an estimated 2327 Wingman35 Crossing Catheters due to suspected tip splitting and consequential risks of injury, internal laceration and bacterial infection, all serious health hazards. FDA: http://ht.ly/UdCY30bCptV

Direct link: https://www.fda.gov/Safety/Recalls/ucm556525.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Catheters are subject to this recall:

Hyland’s Baby Teething Tablet Recall [Australia]

Australia/Canberra: Kadac Pty Ltd. recalls certain batch/lots of Hyland’s Baby Teething Tablets and Hyland’s Baby Nighttime Teething Tablets due to suspected inconsistent amounts of Belladonna Alkaloids, a serious health hazard. ACCC: http://ht.ly/Vvmu30bls2l

Direct link: https://www.productsafety.gov.au/recall/kadac-pty-ltd-hylands-baby-teething-tablets-and-nighttime-teething-tablets

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following drugs are subject to this recall:

Target Egg & Dino Toy Recall [US]

US/Washington: Target recalls an estimated 560,000 Water Absorbing Toys due to risk of ingestion and consequential choking, GI blockage and intestinal obstruction hazards. CPSC: http://ht.ly/xUeY30bkUkN

Direct link: https://www.cpsc.gov/Recalls/2017/Target-Recalls-Water-Absorbing-Toys

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Hatch & Grow Easter Eggs, Easter Grow Toys and Hatch Your Own Dino Toys.

Organic Herbal Nutritional Supplement Recall [US]

US/Silver Spring: Organic Herbal Supply, Inc. recalls certain batch/lots of Uproar, Cummor, Zrect, Monkey Business, Xrect, Rectalis, Tornado, Zdaily, BigNHard, Enhancerol Natural Male Enhancement Supplement capsules due to suspected undeclared  Tadalafil, a FDA-approved drug used as treatment for male Erectile Dysfunction (“ED”). FDA: http://ht.ly/BcXS30b681F

Direct link: https://www.fda.gov/Safety/Recalls/ucm553631.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Nutritional Supplements are subject to this recall:

CHI Tea Tree Blow Dry Primer Lotion Recall [Canada]

Canada/Ottawa: Farouk Systems Inc. recalls an estimated 680 boxed tubes of CHI Tea Tree Blow Dry Primer Lotion due to excessive levels of Methylisothiazolinone (“MI”) and consequential risk of allergic reaction and skin irritation, both serious health hazards. HCSC: http://ht.ly/j0P630b0P6Z

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/62976r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Lotions are subject to this recall:

Hyland’s Baby Teething Tablet Recall [US]

US/Silver Spring: Standard Homeopathic Company recalls certain batch/lots of Hyland’s Baby Teething Tablets and Hyland’s Baby Nighttime Teething Tablets due to suspected inconsistent amounts of Belladonna Alkaloids, a serious health hazard. FDA: http://ht.ly/SWbN30aSox5

Direct link: https://www.fda.gov/Safety/Recalls/ucm552934.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following drugs are subject to this recall:

EpiPen Auto-Injector Recall [US]

US/Silver Spring: Mylan recalls numerous batch/lots of EpiPen Auto-Injectors due to suspected component failure and consequential risk of operational failure during Anaphylaxis treatment, a serious health and safety hazard. FDA: http://ht.ly/zHCZ30ata5a

Direct link: https://www.fda.gov/Safety/Recalls/ucm550173.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following EpiPen Auto-Injector devices are subject to this recall (in alphabetical order):