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.
Showing 2081–2100 of 29,298 recalls
Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...
The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Airway adapter does not meet specification and may break off when attaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Airway adapter does not meet specification and may break off when attaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: A problem was discovered during the scanning process of the outer carton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ORTHO TRAUMA CDS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW Recalled by MEDLINE...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.