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. 2,437 recalls have been distributed to Iowa in the last 12 months.
Showing 31861–31880 of 49,990 recalls
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashby's Sterling Peanut Butter Landslide Ice Cream Recalled by House Of...
The Issue: House of Flavors, Inc. is voluntarily recalling a limited portion of Ashby's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ultimate Chocolate Chip Cookie Dough Pie Recalled by American Blue Ribbon...
The Issue: Product incorporated cookie dough that was potentially contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sterling Nitrile Sterile Powder Free Exam Gloves Recalled by Halyard Health...
The Issue: Defects: Product may be discolored and brittle resulting in the inability of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...
The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...
The Issue: A review of packaging revealed the seal integrity of the pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...
The Issue: Drapes within the affected lots may include a manufacturing variation that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Market Pantry Peanut Butter Cookies. Net Wt. 10.8 oz (306g) Recalled by...
The Issue: Container of Peanut butter cookies contains an incorrect bottom label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...
The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...
The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...
The Issue: Internal testing has demonstrated that the indicated kit lots produce false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.