Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,358 recalls have been distributed to Iowa in the last 12 months.
Showing 1961–1980 of 28,127 recalls
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) STANDARD D&C...
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) SKIN LESION SET...
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) UNIVERSAL 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) 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) IV PACK SOUTH...
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: 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: Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU...
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) RHINOPLASTY PACK...
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) LABOR AND 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) ANGIO CONSOLIDATED...
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) LARGE BIOPSY PACK...
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: to RES Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to There is a...
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: 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: 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: 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: 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.