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. 1,092 recalls have been distributed to Missouri in the last 12 months.
Showing 11421–11440 of 29,298 recalls
Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare Recalled by RAYSEARCH LABORATORIES AB Due to When performing offline...
The Issue: When performing offline image review in RayCare 2C, RayCare 3A and RayCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Removal Case Assembly Recalled by Wright Medical Technology, Inc. Due...
The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardware removal kit Recalled by Wright Medical Technology, Inc. Due to...
The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 40cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.