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. 1,889 recalls have been distributed to Missouri in the last 12 months.
Showing 27261–27280 of 29,298 recalls
Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...
The Issue: In rare instances, channel shifted results have been generated with cobas¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...
The Issue: Product is being recalled because the combination of the current 50 mg vial,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...
The Issue: The current Century Break patch did not contain the same setting for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...
The Issue: Correction to provide clarification and additional labeling to minimize...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Single Stage Embryo Replacement Catheter Product Code:...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMend Absorbable Collagen Membrane BioMend¿ Absorbable Collagen Membrane...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters (with...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Layershield Adhesion Barrier Matrix Layershield Adhesion Barrier Matrix is...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...
The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuraGen Nerve Guide NeuraGen Nerve Guide is indicated for repair Recalled...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Obturator Product...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Absorbable Collagen Sponge Provided As Intermediate to Another Company...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.