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. 2,616 recalls have been distributed to Iowa in the last 12 months.
Showing 10521–10540 of 28,127 recalls
Recalled Item: MicroScan Pos MIC Panel Type 34 - Product Usage: For Recalled by Beckman...
The Issue: Due to a customer report and internal investigation, it was confirmed that a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...
The Issue: The rotating luer fitting at the distal end of the delivery system handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...
The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Recalled by Siemens Medical...
The Issue: When the user changes frame rates from lower frequency (e.g. 10 f/s) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific lots...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Fixed Lateral Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Cancellous Thread Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Trac System Thinflap 24 MM Burr Hole Plate Recalled by Biomet, Inc....
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOENIX Recalled by Biomet, Inc. Due to Specific lots of multiple sterile...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/H MODULAR STEM Recalled by Biomet, Inc. Due to Specific lots of multiple...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Polyethylene Tibial Bushing Recalled by Biomet, Inc. Due to Specific...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RINGLOC BIPOLAR Hip System Bi Polar Locking Ring Recalled by Biomet, Inc....
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder System Recalled by Biomet, Inc. Due to...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0/5.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.