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 81818200 of 49,990 recalls

Medical DeviceAugust 10, 2023· ETHICON, LLC

Recalled Item: PDS II (polydioxanone) Suture Recalled by ETHICON, LLC Due to Internal...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Connex Spot Monitor Recalled by Baxter Healthcare Corporation...

The Issue: Product is being recalled due to the improper placement of a copper tape on...

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

Class II — Potential Health HazardOngoing
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: activator concentrate Recalled by Ecometics, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: Lugol's (Strong Iodine Solution USP) Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: AstrinGyn (Ferric Subsulfate) Aqueous Recalled by Ecometics, Inc. Due to...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: ALCOLADO RELAMPAGO (Menthol and Camphor) Recalled by Ecometics, Inc. Due to...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: Blis-To-Sol Liquid (Tolnaftate) Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: Unguentine Ointment Recalled by Ecometics, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2023· Ecometics, Inc.

Recalled Item: YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively...

The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2023· O&M HALYARD, INC.

Recalled Item: FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with...

The Issue: One respirator sample failed a filtration efficiency test. This respirator...

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

Class II — Potential Health HazardOngoing
FoodAugust 8, 2023· Bickel's Snack Foods Inc

Recalled Item: Butter Flavored Popcorn Naturally & Artificially Flavored Recalled by...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2023· FX SHOULDER

Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...

The Issue: Centered glenosphere box may contain an eccentric glenosphere.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 10ML SYRINGE LUER LOCK W/NEEDLE Recalled by Fresenius Medical Care Holdings,...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...

The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Oculus Optikgeraete GMBH

Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...

The Issue: Their is a potential that optical devices with insufficient anti- coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Oculus Optikgeraete GMBH

Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...

The Issue: Their is a potential that optical devices with insufficient anti- coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Oculus Optikgeraete GMBH

Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...

The Issue: Their is a potential that optical devices with insufficient anti- coating...

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

Class II — Potential Health HazardOngoing