Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,498 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,498 in last 12 months

Showing 1238112400 of 27,852 recalls

Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 23G PFC Injection Needle- .D01 GTIN: 8719214221362 Recalled by Vitreq...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 23G Silicone Tipped Cannula-CN23.D01 GTIN: 8719214221508 Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G PFC Injection Needle-.D01 GTIN: 8719214221386 Recalled by Vitreq...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Pick Needles-.D04 GTIN: 8719214221607 Recalled by Vitreq Bv Due...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Blunt Needles with luer-lock connector-.D05 GTIN: Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G VFI Cannula-.D03 GTIN: 8719214221461 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1) VitreQ 20G BF Blunt Needles-.D51 GTIN: 8719214221089 (2) Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G Blunt Needles with luer-lock connector-.D05 GTIN:8719214221669...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...

The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...

The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...

The Issue: Due to customer reports it has been determined that the inoculation system...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...

The Issue: There is the potential for water to flood the column and enter the circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...

The Issue: There is the potential for water to flood the column and enter the circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing