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. 1,776 recalls have been distributed to Wisconsin in the last 12 months.
Showing 51101–51120 of 52,482 recalls
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...
The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR220amx Mobile general purpose radiographic imaging of the human...
The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromovision High Definition (HD) Wireless Camera Recalled by Berchtold...
The Issue: Defective camera: There is a possibility that the connection of the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRISpec" CA/CB two-part urine chemistry control twin set Recalled by Iris...
The Issue: The firm recalled after it received complaints of IRISpec CA/CB two part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: Recalled...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Recalled by Sentec AG Due to SenTec is recalling a number of V-Sign"2...
The Issue: SenTec is recalling a number of V-Sign"2 Sensors due to a problem regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage:...
The Issue: Digital Skin Mammography Marker separating from the backing of the spot material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyro-Tab 0.137 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.088 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.300 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...
The Issue: cGMP Deviations; does not meet in process specification requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.