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. 1,894 recalls have been distributed to Missouri in the last 12 months.
Showing 26161–26180 of 29,298 recalls
Recalled Item: PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONE-PIECE LAG SCREW 11MM. Item codes starting with 00225900. Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II KEYLESS TUBE Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I/B II KNEE DOMED PATELLA Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN R-F IM NAIL 9MM DIA Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation identified that the design of the drill bit may make the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...
The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...
The Issue: Ortho Clinical Diagnostics issued a product correction notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Respiratory Virus Plus Nucleic Acid Test (RV+) on Recalled by...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...
The Issue: Stryker received two reports indicating that during screw insertion under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of...
The Issue: A review of complaints identified a trend for drills breaking.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...
The Issue: There is a risk that the introducer needles packaged within the kits can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral...
The Issue: A labeling inconsistency was discovered in which the lidstock states that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.