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. 2,488 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,488 in last 12 months

Showing 2048120500 of 28,127 recalls

Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· AGFA Healthcare Corp.

Recalled Item: AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for...

The Issue: The DX-D100 User Manual already contained information about to move a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Hill-Rom, Inc.

Recalled Item: Hill-Rom Bariatric Power Recliner Recalled by Hill-Rom, Inc. Due to The...

The Issue: The recliners were shipped without the foot rest ottoman linkage side...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing