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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels, USA

1 year ago •source fda.gov • details

Baxter International Inc. is voluntarily recalling one lot of Heparin Sodium in 0.9% Sodium Chloride Injection to the consumer level due to the potential for elevated endotoxin levels based on issues related to the bacterial endotoxin test specific to lot number. This issue affects one lot of… See more

#recall #drugs #unitedstates

Recalls Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels Baxter Internat... photo #1
312   Comments Comment

Recall notice

Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings, USA

1 year ago •source fda.gov • details

Abbott has initiated a voluntary medical device correction for a small number of FreeStyle Libre® 3 sensors due to sensors may provide incorrect high glucose readings. The product was distributed in the United States during the first half of May 2024.

The FreeStyle Libre 3 system includes… See more

#recall #medicaldevices #unitedstates

Recalls Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings Abbott has initiated... photo #1
312   Comments Comment

Recall notice

Healthy Living Migraine Relief Tablets - recalled due to Mislabeling, USA

1 year ago •source fda.gov • details

Aurobindo Pharma USA, Inc., on behalf of AuroHealth, is voluntarily recalling one lot of Healthy Living Migraine Relief, Acetaminophen, Aspirin & Caffeine tablets to the consumer level due to the product missing the manufacturer label. The product was distributed through Amazon to be known within the US… See more

#drugs #recall #unitedstates

Recalls Healthy Living Migraine Relief Tablets - recalled due to Mislabeling Aurobindo Pharma USA, Inc., on... photo #1
312   Comments Comment

Recall notice

Umary Hyaluronic Acid, Food Supplement - recalled due to Undeclared Drug Ingredients, USA

1 year ago •source fda.gov • details

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

#vitamins #recall #unitedstates

Recalls Umary Acido Hialuronico, Suplemento Alimenticio - recalled due to Undeclared Drug Ingredients Main P... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence Hikma Pharmaceuticals U... photo #1
312   Comments Comment

Recall notice

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling, USA

1 year ago •source fda.gov • details

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

#drugs #recall #unitedstates

Recalls Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling Endo USA, Inc. is voluntarily... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Volara System Single-Patient Use Circuit and Blue Ventilator Adapter recalled for Handset Plug Issue... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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

#vitamins #drugs #recall #unitedstates

Recalls Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients GURU INC.... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients SoloVital.com is volu... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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

#vitamins #recall #unitedstates

Recalls Hard Steel Capsules & Gold Hard Steel Plus Liquid recalled due to Sildenafil and Acetaminophen Supe... photo #1
312   Comments Comment

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