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. 2,685 recalls have been distributed to Missouri in the last 12 months.
Showing 5461–5480 of 29,298 recalls
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTRA GRAY (soft) TURBO PLUS CUPS Recalled by Young Dental Manufacturing I,...
The Issue: one lot of Contra Gray (soft) Turbo Plus Cups Dental Prophylaxis Angles may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...
The Issue: If "Clear All" selected medications is selected on patient profile, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...
The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...
The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Recalled by...
The Issue: Over-the-needle, intravascular catheters may have needles that do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor with VAMP System Recalled by Edwards Lifesciences, LLC Due...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruWave with Vamp System Pressure monitoring set Recalled by Edwards...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor with Vamp System Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...
The Issue: Potential for damaged and frayed power connector plug with repeated bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...
The Issue: Progressa+ beds have the potential for static buildup from the casters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.