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Safety Reports: Recall

Updated:

Real Time Reports

IKEA has announced a recall of specific batches of its IKEA 365+ VÄRDEFULL Garlic Press due to a production error that poses a risk of small metal pieces detaching during use. The affected products were distributed across Ireland.

The recall involves:
- The IKEA 365+ VÄRDEFULL Garlic… See more

#recall #ikea #ireland

Vita Warehouse Corp. is voluntarily recalling one lot of Welby® brand Vitamin B12 Energy Support gummy product 1000 mcg 140 gummies, Berkely Jensen® Vitamin B12 1000 mcg 250 Gummies, and VitaGlobe™ Vitamin B12 Extra Strength 60 Gummies due to the potential presence of undeclared peanuts. People with… See more

#peanutallergy #recall #unitedstates

Weleda is recalling a batch of its Baby Teething Powder due to the possible presence of glass pieces. The affected product was distributed to various retailers and wholesalers across Ireland.

The recall involves:
- Weleda Baby Teething Powder
- 60g pack size
- With batch code 231302… See more

#recall #ireland

Medtronic issued a voluntary recall notification to global customers related to specific Newport™ HT70 and HT70 Plus ventilators and certain related Newport™ service parts. The FDA recently designated this voluntary action by Medtronic as a Class I recall. With this recall, Medtronic is advising the discontinuation of… See more

#recall #medicaldevices #unitedstates

Recall notice

Kids Multivitamin Gummies recalled due to Mislabeling, USA

9 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

#drugs #recall #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

9 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

9 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

#vitamins #fishallergy #recall #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

#vitamins #recall #unitedstates