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. 970 recalls have been distributed to Missouri in the last 12 months.
Showing 38261–38280 of 52,570 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: Recalled...
The Issue: The Synthes Cranial Flap Tube Clamp and Crimping Device for Cranial Tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caramel Caribou Ice Cream Recalled by The Ice Cream Club, Inc. Due to...
The Issue: Product contains undeclared peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DR. VENESSA'S FORMULAS ULTIMATE ANTIOXIDANT TABLETS DIETARY SUPPLEMENT...
The Issue: The dietary supplement contains undeclared milk and crustacean shellfish...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Peas & Carrots Recalled by Lakeside Foods, Inc Due to Potential...
The Issue: The Ohio Department of Agriculture conducted testing on the product and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KAL Brand Amino Acid Complex Recalled by Nutraceutical International...
The Issue: Undeclared allergen, casein is a disclosed ingredient, but the word milk not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of tests associated with the affected lots(...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes...
The Issue: Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRIdian¿ ViewRay¿ Radiation Therapy System Recalled by Viewray Incorporated...
The Issue: ViewRay discovered that in the event that an encoder breaks or fails on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...
The Issue: Product labeling of these sterile guide wires (external carton label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Controls Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego is recalling the Alere Cholestech LDX Multianalyte Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRACLE DIET 30 capsules Recalled by The One Minute Miracle Inc Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIRACLE ROCK 48 capsules Recalled by The One Minute Miracle Inc Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ThruPort Knot Pusher. This device is sold individually (Model KP1) Recalled...
The Issue: The configuration of the slot at the tip of the knot pusher may inhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.