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. 1,938 recalls have been distributed to Wisconsin in the last 12 months.
Showing 24321–24340 of 52,482 recalls
Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Multi-Lenqth Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Core Straight Safety Wire Guide Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: King LTS-D Kit Size 1 Recalled by King Systems Corp. dba Ambu, Inc. Due to...
The Issue: Size 0 products were incorrectly packaged and labeled as a size 1 products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...
The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Recalled by Elekta Limited Due to In rare circumstances, due to...
The Issue: In rare circumstances, due to reasons such as inadequate hospital facility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to...
The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 10 mg* Recalled by Sun Pharmaceutical...
The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...
The Issue: Lack of Assurance of Sterility: Confirmed customer complaints for leaks on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials Recalled...
The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...
The Issue: Abbott internal testing has identified that the Magnesium urine application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M220 F12 surgical microscope The Leica M220 F12 surgical Recalled by...
The Issue: The M220 optics may unintentionally drop into the surgical field, risking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Forest Wild Collection Dark Chocolate bar Recalled by Salmon River Foods...
The Issue: The 1.25 oz Forest Wild Wolf Dark Chocolate bars are recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Curity All Purpose Sponges Recalled by Cardinal Health 200, LLC Due to...
The Issue: Curity All Purpose Sponges were not sterilized and distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexima Duodenal Bend Biliary Stent with Delivery System Recalled by Boston...
The Issue: The sterile barrier may contain packaging seal defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexima Duodenal Bend Biliary Stent with Delivery System Recalled by Boston...
The Issue: The sterile barrier may contain packaging seal defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vergene Amplification Tray - 700uL Recalled by Luminex Corporation Due to On...
The Issue: On lot of VERIGENE(R) BC-GP Utility Kits (20-011-018) were labeled with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.