Product Recalls in Wisconsin
Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,736 recalls have been distributed to Wisconsin in the last 12 months.
Showing 3421–3440 of 52,482 recalls
Recalled Item: AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXperFD20/10 System Code: (1) 722029 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) Recalled by PHILIPS...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXperFD20/15 System Code: (1) 722058 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M12 System Code: (1) 722227 (2) 722231 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 Recalled by PHILIPS...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 System Code: (1) 722038 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 Recalled...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C System Code: (1) 722001 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL Recalled by Teva...
The Issue: Failed Stability Specifications - 12-month stability test result for one of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing device labeling is being updated to strengthen labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...
The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...
The Issue: Potential that the induction seal is not completely sealed to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Large Volume Pump Software, version 5.9.2 and earlier has potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.