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Recalls

Recent Reports

Umary Acido Hialuronico, Suplemento Alimenticio - recalled due to Undeclared Drug Ingredients, USA

2 months ago •source fda.gov • details

Recall notice

Main Products, Inc. is voluntarily recalling all lots of “Umary Acido Hialuronico, Suplemento Alimenticio to the consumer level. FDA laboratory analysis confirmed that UMARY has been found to be tainted with the drug ingredients, diclofenac and omeprazole. Products containing diclofenac and omeprazole cannot be marketed as dietary… See more

#dietarysupplements #recall #us

Umary Acido Hialuronico, Suplemento Alimenticio - recalled due to Undeclared Drug Ingredients photo #1
321

Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence, USA

2 months ago •source fda.gov • details

Recall notice

Hikma Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Acetaminophen Injection to the consumer/user level. The product is being recalled due to the potential presence of a bag labeled Dexmedetomidine HCL Injection (400mcg/100mL) inside the overwrap that is labeled Acetaminophen Injection, 1000mg/100mL, (10mg/mL). The product was… See more

#recall #drugs #us

Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence photo #1
321

Bissell Steam Shot Handheld Steam Cleaner recalled due to Burn Hazard, USA

2 months ago •source support.bissell.com • details

Recall notice

BISSELL, in cooperation with the Consumer Product Safety Commission (CPSC) and Health Canada, is recalling over 3 million of its Steam Shot™ Handheld Steam Cleaners due to a risk of causing burns by spewing hot water. The affected products were sold in the U.S. and Canada.

The… See more

#us

Bissell Steam Shot Handheld Steam Cleaner recalled due to Burn Hazard photo #1
319

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling, USA

2 months ago •source fda.gov • details

Recall notice

Endo USA, Inc. is voluntarily recalling one lot of Clonazepam Orally Disintegrating Tablets to the consumer level. The product lot is being recalled due to mislabeling where an incorrect strength appears on the cartons. The product lot was distributed through wholesale distributors to retail pharmacies nationwide.

Risk… See more

#recall #drugs #us

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling photo #1
319

Volara System Single-Patient Use Circuit and Blue Ventilator Adapter recalled for Handset Plug Issue, USA

2 months ago •source fda.gov • details

Recall notice

Baxter International Inc. issued an Urgent Medical Device Recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly. The recall is due to reports of the handset plug disconnecting from the nebulizer port on the blue ventilator adapter. The impacted accessories… See more

#recall #medicaldevices #us

Volara System Single-Patient Use Circuit and Blue Ventilator Adapter recalled for Handset Plug Issue photo #1
319

Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients, USA

2 months ago •source fda.gov • details

Recall notice

GURU INC. is voluntarily recalling Infla-650 Herbal Dietary Supplement Capsules, Lot No. IN-032, 700 mg to the consumer/user level. Infla-650 capsules has been found to be tainted with acetaminophen, diclofenac and phenylbutazone, which are not listed on the label. Products containing acetaminophen, diclofenac and phenylbutazone cannot be… See more

#drugs #recall #dietarysupplements #us

Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients photo #1
319

Volara system single-patient use circuit and blue ventilator adapter assembly - recalled due to quality issues, USA

2 months ago •source fda.gov • details

Recall notice

Baxter International Inc. announced today it has issued an Urgent Medical Device Recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly. The recall is due to reports of the handset plug disconnecting from the nebulizer port on the blue ventilator… See more

#medicaldevices #us

Volara system single-patient use circuit and blue ventilator adapter assembly - recalled due to quality issues photo #1
319

Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients, USA

2 months ago •source fda.gov • details

Recall notice

SoloVital.com is voluntarily recalling all lots of Umary Acido Hialuronica, Suplemento Alimenticio – 30 Capletas de 850mg to the consumer level. FDA laboratory analysis confirmed that UMARY has been found to be tainted with the drug ingredients, diclofenac and omeprazole. Products containing diclofenac and omeprazole drug cannot… See more

#recall #drugs #us

Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients photo #1
319

NUXE Very Rose 3 in 1 Soothing Micellar Water recalled due to Bacteria Presence, France

2 months ago •source rappel.conso.gouv.fr • details

Recall notice

Nuxe has voluntarily recalled its Very Rose Eau Micellaire Apaisante 3-en-1 cosmetic product due to the potential presence of the Burkholderia Cepacia bacteria. The product was distributed across France in pharmacies, parapharmacies, online, and selective distributors. This bacteria could cause infections in exceptional cases, particularly in immunocompromised… See more

#fr #bacterial

NUXE Very Rose 3 in 1 Soothing Micellar Water recalled due to Bacteria Presence photo #1
33

Hard Steel Capsules & Gold Hard Steel Plus Liquid recalled due to Sildenafil and Acetaminophen, USA

2 months ago •source fda.gov • details

Recall notice

Supercore Products Group is voluntarily recalling of Hard Steel Capsules & Gold Hard Steel Plus Liquid to the consumer level. FDA analysis has found these products to be tainted with Sildenafil and acetaminophen. Hard Steel is sold worldwide online via their website.

Risk Statement: Consumption of products… See more

#recall #dietarysupplements #us

Hard Steel Capsules & Gold Hard Steel Plus Liquid recalled due to Sildenafil and Acetaminophen photo #1
319

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