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. 2,024 recalls have been distributed to Illinois in the last 12 months.
Showing 21021–21040 of 30,032 recalls
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK TWIST D 3.5X90MM 30MM Can 12MM Rnd Recalled by Zimmer Gmbh Due to...
The Issue: Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Air 205 Recalled by Moller Vital Due to Potential for the bolt on the...
The Issue: Potential for the bolt on the suspension coupling on the Molift Air to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide Recalled by Cook Inc. Due to...
The Issue: Potential coating contamination with glass particles.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.3MM Tapered Router Recalled by Stryker Instruments Div. of Stryker...
The Issue: A variation in flute depth on the routers was observed. The variation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter is issuing a safety alert in response to postmarketing reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...
The Issue: It was reported that the secondary locking mechanism, and its corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...
The Issue: Incorrect CO2 readings with some patient monitors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...
The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...
The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOCOMP6 XPS High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOCOMP6 XP High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Chamber Container fill with gravity/attached transfer sets Recalled by...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.