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. 2,459 recalls have been distributed to Iowa in the last 12 months.
Showing 24381–24400 of 49,990 recalls
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The products labeling contains inconsistencies. In certain instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StageOne Hip Recalled by Zimmer Biomet, Inc. Due to There is a potential for...
The Issue: There is a potential for comingling of the 43MM and 51 MM molds
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to Robust...
The Issue: Robust optimization for plans using beam set + background dose is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...
The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meropenem for Injection Recalled by Pfizer Inc. Due to Lack of assurance of...
The Issue: Lack of assurance of sterility: loss of container integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle...
The Issue: CGMP Deviations; rejected product was used to manufacture final bulk lot
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formed Hash Brown Patties Recalled by Lamb Weston Inc Due to Hash brown...
The Issue: Hash brown product, sold under brands Brookshire's, Market Pantry,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Murry's Hash Brown Potato Patties Recalled by Lamb Weston Inc Due to Hash...
The Issue: Hash brown product, sold under brand Murry's is recalled because the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...
The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....
The Issue: Any change made to current ultrasound machine software or hardware upgrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...
The Issue: Lack of assurance of sterility -Reports of loose metal ferrule crimps on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altavera Levonorgestrel and Ethinyl Estradiol Tablets Recalled by Xiromed...
The Issue: Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SparkleFresh Fluoride Toothpaste Recalled by Medline Industries Inc Due to...
The Issue: Microbial Contamination of Non-Sterile Product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.