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. 1,055 recalls have been distributed to Illinois in the last 12 months.
Showing 30761–30780 of 55,304 recalls
Recalled Item: Amoxicillin and Clavulanate Potassium for Oral Suspension Recalled by Morton...
The Issue: Presence of Foreign Substance: customer complaint of blue foreign material...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alaris Pump Module model 8100 manufactured between November 2011 and March...
The Issue: The recalling firm has received reports of increased or decreased flows that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Synchromed II Model 8637 supplied in 20mL and 40 Recalled by...
The Issue: Medtronic implemented a final design change intended to address the motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVOLVE ADVANCED ADIPOSE SYSTEM Recalled by LifeCell Corporation, A Wholly...
The Issue: Presence of bacterial endotoxins levels above the acceptable limit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Hip Application (THA) Product Usage: The Robotic Arm Interactive...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Right Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.