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. 2,137 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,137 in last 12 months

Showing 44614480 of 52,570 recalls

Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard ANGIOGRAPHY DRAPE PACK - Medical convenience kits Model Number:...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard ORTHO PACK -Medical convenience kits Model Number: MMOK006-04...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard LAPAROTOMY GYN PACK - Medical convenience kits Model Number:...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard FOOT ANKLE PACK - Medical convenience kits Model Number: EUOR005-02...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard MAJOR VAGINAL GYN PACK - Medical convenience kits Model Recalled by...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard CPT EP PACK - Medical convenience kits Model Number: SHAN442-04...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard ENT - Medical convenience kits Model Number: VMED011-01 Recalled by...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard C SECTION PACK - Medical convenience kits Model Number: SJCS66-02...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard GYN TRAY - Medical convenience kits Model Number: LANC014-19...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Covidien LP

Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...

The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
FoodSeptember 19, 2024· HP Hood LLC

Recalled Item: Lactaid Lactose Reduced milk 1. 96 oz Lactaid Whole Milk Recalled by HP Hood...

The Issue: Milk may contain undeclared almond from almond milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 19, 2024· Gilead Sciences, Inc.

Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: Presence of glass particle.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...

The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...

The Issue: To better define the drying procedures described in the IFU to improve the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Baxter Healthcare Corporation

Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...

The Issue: The beds have a potential for an interface issue with the Rauland Responder...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· American Surgical Company, LLC

Recalled Item: Americot 20-01S (1/4" x 1/4") or 6mm x 6mm: Neurological Recalled by...

The Issue: Product defect where the X-ray detectable barium strip (aka radio-opaque...

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

Class II — Potential Health HazardOngoing