Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,711 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,711 in last 12 months

Showing 27812800 of 13,409 recalls

DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Manufacturing deviations were reported due to an abnormal...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2022· Akorn, Inc.

Recalled Item: Olopatadine HCl Recalled by Akorn, Inc. Due to Failed impurity/degradation...

The Issue: Failed impurity/degradation specifications: Out of specification for 2-HMP...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: lots made with same active pharmaceutical ingredient (API)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Tablet/Capsule Specification; oversized tablet found in a bottle

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 24, 2022· Grato Holdings, Inc.

Recalled Item: Homeopathic EarAche Drops Recalled by Grato Holdings, Inc. Due to Microbial...

The Issue: Microbial contamination of non-sterile product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri Ajo King con Ortiga y Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 24, 2022· Grato Holdings, Inc.

Recalled Item: Homeopathic EarAche Ear Drops Recalled by Grato Holdings, Inc. Due to...

The Issue: Microbial contamination of non-sterile product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· US Specialty Formulations LLC

Recalled Item: B-Complex + Chromic Chloride (Choline Chloride 3% Recalled by US Specialty...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· US Specialty Formulations LLC

Recalled Item: Ethanol for Injection 95% Recalled by US Specialty Formulations LLC Due to...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Grato Holdings, Inc.

Recalled Item: Earache Drops Recalled by Grato Holdings, Inc. Due to Microbial...

The Issue: Microbial contamination of non-sterile product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Fentanyl Citrate in 0.9% Sodium Chloride Injection Recalled by Nephron...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Alprostadil Injection USP 500 mcg/mL Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications; out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund