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. 2,622 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,622 in last 12 months

Showing 77017720 of 49,990 recalls

Medical DeviceOctober 10, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: Stay Safe Cap Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Updating the labeling to include additional warnings and contraindications...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP Emergency Drive Recalled by Maquet Medical Systems USA Due to...

The Issue: Product removal due to possible blocking or impairment of the CARDIOHELP...

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

Class I — Serious Health HazardOngoing
FoodOctober 9, 2023· Greenhead Lobster Products LLC

Recalled Item: Frozen and fresh RTE Lobster meat (1 lb. packages to Recalled by Greenhead...

The Issue: Lobster meat may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 9, 2023· Betty Lou's Inc

Recalled Item: Stabilyze Sugar Stable Dark Chocolate Peanut Butter Recalled by Betty Lou's...

The Issue: Undeclared Sesame

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2023· Philips North America

Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to This recall is...

The Issue: This recall is part of a 2-issue recall for the same system. When using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing