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 2701–2720 of 52,482 recalls
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Preset treatment parameters are not consistently being used in accordance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...
The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...
The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...
The Issue: Devices for the affected lot were not assembled according to product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...
The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...
The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...
The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...
The Issue: Due to manufacturing issues, abutment products were manufactured with screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HistoCore PELORIS 3 Recalled by Leica Biosystems Melbourne Pty Ltd Due to...
The Issue: There is a leakage issue associated with the tubing in the manifold of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tony's Chocolonely Everything Bar Recalled by TONY'S CHOCOLONELY INC Due to...
The Issue: Contains foreign objects (stones)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tony's Chocolonely Dark Chocolate Almond Sea Salt Recalled by TONY'S...
The Issue: Contains foreign objects (stones)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dr. Praeger s California Veggie Fries 8oz Recalled by Dr. Praeger's Sensible...
The Issue: Undeclared Allergen (Soy)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: myQA iON Recalled by IBA Dosimetry GmbH Due to Wrong analysis results can...
The Issue: Wrong analysis results can occur if the user creates two structures with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance CT Big Bore Recalled by Philips North America Llc Due to...
The Issue: Unintended motion issues related to Interventional Control that may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.