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. 2,644 recalls have been distributed to Iowa in the last 12 months.
Showing 4081–4100 of 49,990 recalls
Recalled Item: MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE NEXUS 19/20G CATH CONNECTOR Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z Recalled by...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat SUV Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Positioner. Model Number C-XP-5000Z Recalled by Maquet...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter AK 98 Dialysis Machine Recalled by Baxter Healthcare Corporation Due...
The Issue: Baxter is aware of several recalls by other manufacturers related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (1) Medline Pacer Implant Pack Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Some of the suture packages within the convenience kits contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Medline Open Heart CDS Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Some of the suture packages within the convenience kits contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Shoulder Repair Pack-LF Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Some of the suture packages within the convenience kits contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...
The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...
The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Home Alone International Delight Peppermint Mocha Zero Sugar Recalled by...
The Issue: The International Delight Zero Sugar Peppermint Mocha is recalled because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Gambler Recalled by Dakota Tom's, Inc Due to Potential Listeria...
The Issue: Potential Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pepperjack Cheese Burger Recalled by Dakota Tom's, Inc Due to Potential...
The Issue: Potential Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bacon Cheeseburger Recalled by Dakota Tom's, Inc Due to Potential Listeria...
The Issue: Potential Listeria monocytogenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triamcinolone Acetonide Cream USP Recalled by Padagis US LLC Due to...
The Issue: Subpotent and Superpotent Drug. Out of specification assay results recorded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4.5 x 180 mm Aggressive Cutter Recalled by Karl Storz Endoscopy Due to Due...
The Issue: Due to holes detected in the inner barrier system that may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.