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. 2,515 recalls have been distributed to Wisconsin in the last 12 months.
Showing 27441–27460 of 28,744 recalls
Recalled Item: Quasar Power Pack contains a Baby Quasar and a Baby Recalled by Quasar...
The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...
The Issue: A manufacturing defect has been identified which could results in the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Quasar (LAB-001-D Recalled by Quasar Bio-Tech, Inc. dba Silver Bay LLC...
The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers...
The Issue: When the operator for a wall stand view selects an "image rotation"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that...
The Issue: Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...
The Issue: A manufacturing defect has been identified which could results in the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlant Recalled by Kerr Corporation Due to The firm initiated the recall...
The Issue: The firm initiated the recall becaue disturbing the BioPlant product soon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical Systems Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Software anomaly. Philips determined that the TumorLOC software program for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical Systems Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Software anomaly. Philips determined that the TumorLOC software program for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge.115mmx115mm Pledget Recalled...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...
The Issue: The recall was initiated because Superstat Corporation has confirmed that no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical Systems Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Software anomaly. Philips determined that the TumorLOC software program for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.