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. 1,855 recalls have been distributed to Wisconsin in the last 12 months.
Showing 36921–36940 of 52,482 recalls
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...
The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: InVision-Plus CS Needleless IV Connector Recalled by Rymed Technologies, LLC...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters Recalled...
The Issue: Report by a customer of an open package seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.