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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Kids Multivitamin Gummies recalled due to Mislabeling, USA

7 months ago source accessdata.fda.gov details

Nordic Naturals has issued a recall for its Zero Sugar Kids Multivitamin Gummies due to mislabeling. The recall affects products distributed domestically in AK, AZ, CA, CO, FL, GA, ID, IN, MA, MT, NC, ND, NH, NV, NY, OK, OR, RI, UT, WA, and internationally to Great… See more

#recall #unitedstates

Church & Dwight Co., Inc. is voluntarily recalling all lots within expiry of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs to the consumer level. The products are being recalled due to potential microbial contamination identified as fungi in cotton swab… See more

#recall #drugs #unitedstates

Smiths Medical has issued a recall for certain CADD-Solis Ambulatory Infusion Pumps due to potential thermal damage issues. The recall affects devices distributed for use in hospital and homecare settings. The FDA has classified this as a serious recall.

The recall was initiated after Smiths Medical identified… See more

#recall #unitedstates

Recall notice

Dervivea Metal Jewellery recalled due to Chemical Risk, UK

7 months ago source gov.uk details

The Office for Product Safety and Standards has issued a recall for Dervivea Metal Jewellery sold on Amazon due to a serious chemical risk as the cadmium content was found to be greater than the maximum permissible limit in both the metal ring and metal earrings. The… See more

#recall #unitedkingdom

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Recall notice

GNC Women's 30+ Vitapak recalled due to Undeclared Fish Allergen, USA

7 months ago source accessdata.fda.gov details

GNC Holdings LLC has issued a recall for its Women's 30+ Vitapak due to an undeclared fish allergen, parvalbumin. The product was distributed across multiple states including AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD,… See more

#recall #supplement #allergicreaction #unitedstates

Amneal Pharmaceutical LLC, is recalling three lots of Sulfamethoxazole/Trimethoprim Tablets, USP, 400 mg/80 mg to the consumer level as the tablets may exhibit black spots on the tablet surface due to microbial contamination. The observance of black spots was reported in a product quality complaint. The recalled… See more

#supplement #recall #unitedstates

Recall notice

AVKARE Eye Drops Recalled Over Sterility Issues, United States

7 months ago source avkare.com details

BRS Analytical Service, LLC. has initiated a voluntary recall of various ophthalmic products due to manufacturing deviations identified during an FDA audit. The potential health hazard to users is currently unknown, but the deviations may lead to products of unacceptable quality. The recall was initiated after the… See more

#drugs #recall #unitedstates

The FDA is alerting consumers, tattoo artists, and retailers of the potential for serious injury from use of tattoo inks that are contaminated with bacteria, including Pseudomonas aeruginosa. The affected products were distributed across the US.

Tattoo inks contaminated with pathogenic microorganisms can cause infections and lead… See more

#recall #cosmetics #unitedstates

HEALTH FIXER is voluntarily recalling all lots of dietary supplements by the name of Male Ultra, Malextra, Electro Buzz, Ultra Armor and Male Ultra Pro- blister packs of 10 capsules per box/carton to the consumer level. Laboratory analysis has found the products to be tainted with chloropretadalafil,… See more

#recall #dietarysupplements #unitedstates

CRONUS PHARMA LLC, on behalf of Cronus Pharma Specialties, Hyderabad, India is issuing a voluntary recall involving one batch comprising two distinct lots: Dexased™ (Aspen) and Dexmedvet™ (Cronus Pharma LLC). Both products contain Dexmedetomidine Hydrochloride Injection 0.5 mg/mL, which is a prescription product in the United States… See more

#recall #animalveterinary #unitedstates