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. 2,422 recalls have been distributed to Iowa in the last 12 months.
Showing 35241–35260 of 49,990 recalls
Recalled Item: Custard Bismark 9999954007 Recalled by Kwik Trip Bakery Due to Kwik Trip,...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KBS Plain Bagel Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc. is...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jelly Bismark 9999954008 Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc....
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cinnamon Cinnsations Recalled by Kwik Trip Bakery Due to Kwik Trip, Inc. is...
The Issue: Kwik Trip, Inc. is recalling various bakery goods which might be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IMMULITE 2000 EstradiolTest Code E2 Catalog Number: L2KE22 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number:...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Estradiol Test Code E2 Catalog Number: LKE21 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Estradiol Test Code E2 Catalog Number: K6463 Recalled...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF...
The Issue: The Firm has discovered a Software bug.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ice Nuggets Recalled by Kwik Trip, Inc. Due to Kwik Trip Inc reported a...
The Issue: Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Super Arrow-Flex Percutaneous Sheath Introducer Sets or CL-07635 Recalled by...
The Issue: Arrow has issued a recall for these products due to potential packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leica Microsystems (Schweiz) Ag. The common name of the device Recalled by...
The Issue: An electronic component of the Leica M525 OH4 and Leica M720 OH5 surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 25 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 48 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 12 consists of all product under product code JDI Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 31 consists of all product under product code: KTT Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 29 consists of all product under product code: LPHand Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 52 consists of product code: HWC and same usage: Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.