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 24581–24600 of 49,990 recalls
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...
The Issue: The device has an offset in the design that results in a reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...
The Issue: The reagent pack exhibits the potential for an increased frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due...
The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due...
The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241-S Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...
The Issue: There is a potential to generate falsely elevated serum or plasma chloride...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...
The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...
The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroid Recalled by Humco Holding Group, Inc Due to CGMP Deviations: Recall...
The Issue: CGMP Deviations: Recall notice received from supplier that Thyroid Powder...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.