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. 2,489 recalls have been distributed to Iowa in the last 12 months.
Showing 20421–20440 of 49,990 recalls
Recalled Item: GENTLEWAVE Recalled by Sonendo Inc Due to The console would continue to run...
The Issue: The console would continue to run for extended period when the foot pedal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Carbon Dioxide Reagent Kit Recalled by Abbott GmBH & Co. KG Due to...
The Issue: Abbott internal studies have determined that atmospheric Carbon Dioxide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cool Mint Tablets Maximum Strength Zantac 150 mg Sanofi Distributed by:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Zantac 150 mg Distributed by: Chattem Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cool Mint Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 150 mg Distributed by: Chattem Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Vaginal Inserts USP Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective Delivery System: complaints for difficulty in pushing the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...
The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...
The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...
The Issue: Potential for the incorrect pressure safety valve being included in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...
The Issue: Their is a possibility that the cannula may separate from its connector,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals...
The Issue: Incorrect labeling: Incorrect or missing lot and/or exp date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.