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. 2,660 recalls have been distributed to Iowa in the last 12 months.
Showing 2701–2720 of 28,127 recalls
Recalled Item: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE...
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) ECHOSTIM BLOCK SET 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 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: (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: 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.
Recalled Item: VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively...
The Issue: May Generate Negatively Biased Results When Testing Samples with High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioZorb Marker. Radiographic soft tissue marker. Recalled by Hologic, Inc...
The Issue: Firm received reports of adverse events/complications that include serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to Recalled by...
The Issue: A software issue affecting Philips Vue PACS may cause incorrect ischemic map...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: PORT INSERTION PACK Recalled by MEDLINE...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.