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. 2,677 recalls have been distributed to Illinois in the last 12 months.
Showing 41281–41300 of 55,304 recalls
Recalled Item: ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision RXi Digital system Recalled by GE Healthcare Due to...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP PS TB TRL SZ10 INTENDED USE: The Recalled by DePuy...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP CR ARTICULATION SURFACE SZ1 Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A reported incident of a...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and...
The Issue: The SFD/IDD safety mechanism may not engage properly at the lower range of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...
The Issue: QC results were out of range resulting in false resistant strains.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...
The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXYCODONE HCl C-II Tablets Recalled by The Harvard Drug Group, LLC Due to...
The Issue: Superpotent Drug: Confirmed customer complaint of a single unit dose blister...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEXIUM¿ (esomeprazole magnesium) Recalled by AstraZeneca Pharmaceuticals LP...
The Issue: Presence of Foreign Tablets/Capsules: Confimed customer compliant by a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Garden Fresh Steakhouse Potato Salad Kit Recalled by Garden-Fresh Foods,...
The Issue: Garden Fresh Foods, Inc. reported one case of Steakhouse Potato Salad Kit...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diet Bubba Cola Recalled by Dr. Pepper Snapple Group Inc Due to The firm was...
The Issue: The firm was notified by one of it's retail stores that the ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...
The Issue: There is a potential issue that could result to collision between the C-arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...
The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Femoral Alignment Guide 4mm x 6¿ Recalled by Omnilife Science Inc....
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Femoral Alignment Guide Recalled by Omnilife Science Inc. Due to The...
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.