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. 1,209 recalls have been distributed to Illinois in the last 12 months.
Showing 1601–1620 of 30,032 recalls
Recalled Item: Model SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an email to...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number 40KWFXPLUS-710CW.007 Recalled by SEDECAL SA Due to Sedecal sent...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number 40KW-FX.899 Recalled by SEDECAL SA Due to Sedecal sent an email...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU RF.004 Recalled by SEDECAL SA Due to Sedecal sent an email to its...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number 40KWFXPLUS.004 Recalled by SEDECAL SA Due to Sedecal sent an...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number SM-32HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR 2.2 Recalled by SEDECAL SA Due to Sedecal sent an email...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...
The Issue: As a result of a comprehensive product performance review it was determine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...
The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Recalled by DRG...
The Issue: An incoming complaint reported that the expiration date on the kit box label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.