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. 2,571 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,571 in last 12 months

Showing 1412114140 of 28,127 recalls

Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS 4.0 countersink Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS 7.5 tap Recalled by Zimmer GmbH Due to An investigation identified that...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 3.5mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS high Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS 4.5 countersink Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount Recalled...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing