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. 958 recalls have been distributed to Wisconsin in the last 12 months.
Showing 49221–49240 of 52,482 recalls
Recalled Item: Venlafaxine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chicken of the Sea 5-Ounce Chunk Light Tuna in Oil. Recalled by Tri-Union...
The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chicken of the Sea Brand 5-ounce chunk white albacore tuna Recalled by...
The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NeuViz Dual series CT Scanner System Recalled by Philips And Neusoft Medical...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse...
The Issue: The product specifications sheet, part of the Instructions for Use (IFU),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza SW version VA20 with Mammography license. image...
The Issue: Siemens issued a Customer Safety Notice to inform customers of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect QLC1677E Recalled by Steris Corporation Due to During a...
The Issue: During a routine label review, the firm identified four SYSTEM 1E Quick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...
The Issue: An internal review of CareFusion's labeling for preoperative skin prep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...
The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.