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. 1,039 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,039 in last 12 months

Showing 16261–16280 of 48,326 recalls

Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** spineX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Failed pH Specifications: Out of Specification pH Test Results were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2020· AVKARE Inc.

Recalled Item: Sildenafil Tablets USP 100 mg Recalled by AVKARE Inc. Due to Product mix-up:...

The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2020· AVKARE Inc.

Recalled Item: TraZODONE Hydrochloride Tablets USP 100 mg Recalled by AVKARE Inc. Due to...

The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 5, 2020· VISBY MEDICAL INC

Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...

The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...

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

Class II — Potential Health HazardOngoing
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Zydus...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2020· Flowers Foods (Corporate Offices)

Recalled Item: CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ Recalled by...

The Issue: The firm discovered that some of their products showed higher than...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2020· Flowers Foods (Corporate Offices)

Recalled Item: CANYON BAKEHOUSE GLUTEN MOUNTAIN WHITE BREAD NET WT. 18oz (1lb Recalled by...

The Issue: The firm discovered that some of their products showed higher than...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 154 cm (61 IN) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18cm) APPX 0.43ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 60" (152 cm) Appx 1.9 ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Beckman Coulter Inc.

Recalled Item: MicroScan Pos MIC Panel Type 34 - Product Usage: For Recalled by Beckman...

The Issue: Due to a customer report and internal investigation, it was confirmed that a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 9"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing