Product Recalls in Illinois
Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,890 recalls have been distributed to Illinois in the last 12 months.
Showing 10981–11000 of 30,032 recalls
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: 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: RingLoc+ Quick Connect Drill Bit 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: 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.
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: 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: Titanium IFS 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: 6.5/8.0mm 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.
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: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to System...
The Issue: System does not trigger a cancel command followed by a reload of the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.