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. 1,984 recalls have been distributed to Illinois in the last 12 months.
Showing 25281–25300 of 30,032 recalls
Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling
The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...
The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...
The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...
The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF PET/CT16: 882470 Recalled by Philips Medical Systems (Cleveland)...
The Issue: When beginning a procedure to start the gantry and CT Host, a Close Estop ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...
The Issue: Trend in reports of unexpected decrease in beam output in C-series High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...
The Issue: Inadequate iodine and packaging related defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...
The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...
The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS Recalled by Aesculap, Inc. Due...
The Issue: Aesculap Inc. (AIC (USA)) has initiated a voluntary recall of Dafilon Black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...
The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...
The Issue: Two lots of screws were commingled. Screws with etching and machining for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Set Recalled by Medical Action Industries Inc Due to Some of the...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Laceration Kit Recalled by Medical Action Industries Inc Due to Some...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.