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. 2,711 recalls have been distributed to Missouri in the last 12 months.
Showing 1981–2000 of 29,298 recalls
Recalled Item: Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) BASIC CATARACT...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) PAIN PACK Recalled...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) INTUBATION TRAY...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) PRECIP TRAY...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits used for various procedures: 1) DR. KHAN Recalled...
The Issue: There is a potential for open/weak seals on purchased breather pouches used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter NovumIQ Syringe INFUSION SYSTEM Recalled by Baxter Healthcare...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder Stem Recalled by ZIMMER ORTHOPEDICS MANFACTURING...
The Issue: Five complaints received where surgeon was unable to remove and/or connect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoroptor VRx Digital System Model Numbers: 16241 Recalled by Reichert, Inc....
The Issue: The head of the phoropter head could come loose and potentially detach due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoroptor VRx Digital System Model Numbers: 16242 Recalled by Reichert, Inc....
The Issue: The head of the phoropter head could come loose and potentially detach due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim X2 Insulin Pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tandem Mobi Insulin Pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...
The Issue: The hardness not meeting the material specification and may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...
The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration...
The Issue: Aspiration catheter distal tip features and characteristics may not be in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: Beckman Coulter has determined that device software versions V1.3, V1.4,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Da Vinci 5 Product Name: ASSY Recalled by Intuitive Surgical,...
The Issue: Due to an increase in complaints concerning foot tray pedal spring failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otopore Cylinder outer ear wound dressing Recalled by Stryker Corporation...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore FD fragmentable nasal dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otopore Square outer ear wound dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.