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. 2,357 recalls have been distributed to Iowa in the last 12 months.
Showing 48001–48020 of 49,990 recalls
Recalled Item: Hot Pepper Jelly Recalled by Hanover Pike Enterprises, Inc. Due to Undeclared On
The Issue: Food was manufactured with milk and soy ingredients, which are undeclared on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pepper Jelly Recalled by Hanover Pike Enterprises, Inc. Due to Undeclared On
The Issue: Food was manufactured with milk and soy ingredients, which are undeclared on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blackberry Brandy Jam Recalled by Hanover Pike Enterprises, Inc. Due to...
The Issue: Food was manufactured with milk and soy ingredients, which are undeclared on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peach Brandy Jam Recalled by Hanover Pike Enterprises, Inc. Due to Undeclared On
The Issue: Food was manufactured with milk and soy ingredients, which are undeclared on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray V12 Size: 320 mm X 320 mm X 450 Recalled by Mindray DS USA, Inc....
The Issue: Mindray has identified an issue with the V Series Monitor where the monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: An anomaly has been identified with the ARIA Oncology Information System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: We are notifying you of a potential interaction between therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresh Express Leafy Green Romaine Recalled by Fresh Express Incorporated Due...
The Issue: USDA MDP program had a positive sample result for Listeria Monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets USP Recalled by Watson...
The Issue: Superpotent (Multiple Ingredient) Drug: There is the potential for oversized...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 10% Dextrose Injection USP Recalled by Baxter Healthcare Corp. Due to...
The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's Injection USP Recalled by Baxter Healthcare Corp. Due to...
The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection USP Recalled by Baxter Healthcare Corp. Due to...
The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection USP Recalled by Baxter...
The Issue: Chemical Contamination: The IV solutions were packaged in AVIVA containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.