Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,518 recalls have been distributed to Minnesota in the last 12 months.
Showing 20761–20780 of 29,186 recalls
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Confocal GI Scope Product Usage: Intended to provide optical visualization...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...
The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: When taking measurements from images on the Cardio workstation or from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....
The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station and Merge Eye Care PACS. Recalled by Merge Healthcare,...
The Issue: During an antivirus program scan of the Eye Station or Eye Care PACS, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...
The Issue: Use of the software may show an incorrect value to the user when viewing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...
The Issue: An error message can occur resulting in the prior studies being unavailable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Care Systems Recalled by Merge Healthcare, Inc. Due to The system...
The Issue: The system will completely stop allowing the downloading or acquisition of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpO2 connecting cable for Masimo LNCS sensor (Merge Part Number:...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...
The Issue: The study is archived but cannot be opened in iConnect Access and cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...
The Issue: The versions allow images to be stored without pixel data, resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.