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. 2,660 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,660 in last 12 months

Showing 721740 of 49,990 recalls

FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 19927 Kirkland Signature Caesar Salad Recalled by Costco...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Carton label: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA, Inc...

The Issue: Defective Container - A defect in the side-seal which allows leakage of product.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 7, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...

The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...

The Issue: Due to a number of modules flashed with a date and time associated with the...

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

Class II — Potential Health HazardOngoing
DrugNovember 6, 2025· Fresenius Kabi USA, LLC

Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm Recalled by C.R....

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· Bard Peripheral Vascular Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...

The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
DrugNovember 5, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: Sertraline Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....

The Issue: Defective container - seal not adhering to bottles

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100425-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100225-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100220-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100325-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100125-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Diasol, Inc

Recalled Item: Brand Name: Diasol Product Name: 100230-10-DEX100 Recalled by Diasol, Inc...

The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Accriva Diagnostics, Inc.

Recalled Item: Hemochron Activated Clotting Time Low-Range Test Cuvette Recalled by Accriva...

The Issue: Test cuvettes, used with an assay for monitoring heparin anticoagulation,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2025· Cepheid

Recalled Item: Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10. Recalled by Cepheid Due to...

The Issue: Product testing did not meet expected stability criteria.

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

Class II — Potential Health HazardOngoing
FoodNovember 4, 2025· Tai Phat Wholesalers, LLC

Recalled Item: Sofit Recalled by Tai Phat Wholesalers, LLC Due to Undeclared Sulfites

The Issue: Undeclared sulfites

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

Class I — Serious Health HazardOngoing
Refund