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. 1,937 recalls have been distributed to Missouri in the last 12 months.
Showing 21301–21320 of 29,298 recalls
Recalled Item: Wilson Implantation System Product Usage: Indicated to aid in tissue...
The Issue: The firm received a complaint of an open pouch which breaches the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC...
The Issue: The firm received a complaint of an open pouch which breaches the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Direct Supply aluminum crutch Recalled by Medical Depot Inc. Due to Tip...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal aluminum crutch Recalled by Medical Depot Inc. Due to Tip crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...
The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC CHS Plate/Lag Screw Introducer Recalled by Biomet, Inc. Due to A...
The Issue: A complaint was received where the Hiploc Plate/Lag Screw Introducer was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...
The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...
The Issue: Siemens found a defective part in their production line which could increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.