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. 2,590 recalls have been distributed to Iowa in the last 12 months.
Showing 11841–11860 of 28,127 recalls
Recalled Item: Knee Products: 189420 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Products Item Number: 1) 110010462 RingLoc Hip System Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 141356 Regenerex Series-A Patella 3 Peg Recalled by Biomet,...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: The unplugging of the main cable on the monitor trolley from the X10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 183742 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...
The Issue: This product has been confirmed to exhibit holes in the packaging, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...
The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Formula 418 Renal Balloon-Expandable Stent Recalled by Cook Inc. Due to The...
The Issue: The firm received complaints on five devices from one specific lot where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...
The Issue: There is potential for a white paper-type residue attached to the catheter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.