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. 1,150 recalls have been distributed to Missouri in the last 12 months.
Showing 941–960 of 29,298 recalls
Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...
The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical Recalled by Medline Industries, LP Due to Medline has...
The Issue: Medline has identified a limited quantity of saline IV flush syringes that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FERNO POWER X2 POWERED AMBULANCE COT Recalled by Ferno-Washington Inc Due to...
The Issue: The fastening post hardware could loosen allowing the fastening post to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENACIO Pump with InhibiZone Recalled by Boston Scientific Corporation Due...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENACIO Pump without InhibiZone Recalled by Boston Scientific Corporation...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LGX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 Recalled by Olympus Corporation...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 Recalled by Olympus Corporation...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.