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. 1,846 recalls have been distributed to Iowa in the last 12 months.
Showing 27461–27480 of 49,990 recalls
Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...
The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...
The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...
The Issue: The firm made multiple changes to the product requiring the submission of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...
The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating IV Pole Rotating IV Pole falls under the category Recalled by...
The Issue: There is the potential for the Rotating IV Pole to fall. A fall could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bull Capsules Recalled by BYL Solutions Inc. Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from Morphine...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from Fentanyl...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLUE PEARL capsules Recalled by Blue Fusion Natural Due to Undeclared Sildenafil
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by Prinston Pharmaceutical Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: confirmed customer complaint of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZIMMER PATELLA FEMORAL JOINT¿ Osteoarthritis Recalled by Zimmer Biomet, Inc....
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR SIZE 0 STD prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.