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. 2,733 recalls have been distributed to Illinois in the last 12 months.
Showing 27721–27740 of 55,304 recalls
Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...
The Issue: The product was mislabeled with the incorrect label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...
The Issue: Presence of Particulate Matter: organic and inorganic compounds detected in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ...
The Issue: Undeclared allergens on the labeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Revolution CT systems with the SmartStep Option The system is Recalled by GE...
The Issue: On the Revolution CT systems equipped with the SmartStep Option, the Z...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Recalled by...
The Issue: Dental varnish has the possibility of having an unpleasant and off flavor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right Recalled...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left Recalled by...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right Recalled by...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left Recalled by...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left Recalled by...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.