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. 2,459 recalls have been distributed to Iowa in the last 12 months.
Showing 23541–23560 of 28,127 recalls
Recalled Item: Specialty Aria Inserter Recalled by Stryker Spine Due to Stryker has...
The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...
The Issue: In specific situation a partially truncated file may be written to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Unitized Catheter and Accessories...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve only with SIPHONGUARD¿ Device Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Catheter and Accessories Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....
The Issue: There was an error in manufacturing which resulted in the proximal lag screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...
The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...
The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Femoral Boss Reamer Recalled by Biomet, Inc. Due to The...
The Issue: The Vanguard 360 Femoral Boss Reamers were manufactured oversized to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Recalled by...
The Issue: Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.