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. 1,040 recalls have been distributed to Missouri in the last 12 months.
Showing 16141–16160 of 52,570 recalls
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER Recalled by Roche Diagnostics...
The Issue: Roche received several complaints regarding increased control recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concerto User Interface Software provided with the following systems: (1)...
The Issue: If a saved treatment plan with 2 opposing beams is edited prior to approval,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed Visions PV .035 IVUS Catheter Recalled by Northeast...
The Issue: 510k indicated one (1) reprocessing cycle, product not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brew Dr. Uplift Blueberry Raspberry Yerba Mate Guayusa Recalled by BREW DR...
The Issue: Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cooked Snow Crab Recalled by Crustaces Baie-Trinite Inc. Due to Potential...
The Issue: Cooked frozen snow crab sections potentially contaminated with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brew Dr. Uplift Blood Orange Lemon Recalled by BREW DR KOMBUCHA LLC Due to...
The Issue: Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brew Dr. Uplift Mango Passionfruit Recalled by BREW DR KOMBUCHA LLC Due to...
The Issue: Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenia Ambition X - Model Number: 781356 Recalled by Philips North America...
The Issue: The MR magnet is equipped with 4 lifting blocks, which are positioned on top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S - Model Number: 781359 Diagnostic MR system. Recalled by...
The Issue: The MR magnet is equipped with 4 lifting blocks, which are positioned on top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...
The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enoki Mushroom Product of Korea Net Wt. 200 g/7.05 oz. Recalled by GOLDEN...
The Issue: Michigan Department of Agriculture and Rural Development sampled product and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...
The Issue: Removing parts for safety reasons due to possible breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.