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. 2,678 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,678 in last 12 months

Showing 69416960 of 52,570 recalls

DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Niacin Extended-Release Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Niacin Extended-Release Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 80 mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 40mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Zolpidem Tartrate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2024· Henry Schein Inc. and Glove Club HSI Gloves Inc.

Recalled Item: Adrenalin (epinephrine) Injection 1mg/mL Recalled by Henry Schein Inc. and...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2024· Ascend Laboratories, LLC

Recalled Item: Fosfomycin Tromethamine Granules for Oral Solution Recalled by Ascend...

The Issue: Failed Impurities/Degradation Specification: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2024· Den-Mat Holdings, LLC

Recalled Item: Hydrogen Peroxide Oral Rinse Recalled by Den-Mat Holdings, LLC Due to CGMP...

The Issue: CGMP Deviations: products may not conform to the labeled specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2024· Den-Mat Holdings, LLC

Recalled Item: OralProCare medicated lip treatment Recalled by Den-Mat Holdings, LLC Due to...

The Issue: CGMP Deviations: products may not conform to the labeled specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2024· Avanos Medical, Inc.

Recalled Item: MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC*...

The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2024· Avanos Medical, Inc.

Recalled Item: MIC* Gastric-Jejunal Feeding Tube Recalled by Avanos Medical, Inc. Due to...

The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2024· W&H DENTALWERK BUERMOOS GMBH

Recalled Item: W&H Surgical handpiece S-12. For Surgical treatment of dental hard Recalled...

The Issue: 1:2 speed increasing surgical handpieces have been incorrectly laser marked...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2024· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The Emergency...

The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2024· Maquet Medical Systems USA

Recalled Item: Model No. BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The...

The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2024· Olympus Corporation of the Americas

Recalled Item: Water Filter MAJ-2318. This MAJ-2318 water filter has been designed Recalled...

The Issue: Water filter may have been assembled incorrectly, resulting in unfiltered...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 15, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Amneal Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2024· Medical Action Industries, Inc. 306

Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...

The Issue: The kits contain saline flush syringes which were recalled by the supplier.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...

The Issue: When using those products you may experience difficulties to extend or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...

The Issue: When using those products you may experience difficulties to extend or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing