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. 2,456 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,456 in last 12 months

Showing 1850118520 of 48,326 recalls

Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Ion Torrent Dx No Template Control Kit- IVD for detection Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test RNA Control- IVD for detection of Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2020· Aesthetics Biomedical, Inc.

Recalled Item: SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Recalled by...

The Issue: A high frequency output (2 MHz) has not been cleared for distribution in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2020· Biomet, Inc.

Recalled Item: Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips...

The Issue: There were unknown bioburden levels prior to sterilization, which may affect...

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

Class II — Potential Health HazardOngoing
FoodMarch 12, 2020· Advanced Fresh Concepts Corp

Recalled Item: Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp Recalled by Advanced...

The Issue: Firm testing found Vibrio parahaemolyticus in cooked butterfly shrimp from...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Sprout Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Mixed Greens 4 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Spring Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Red Clover 4 oz Recalled by Chicago Indoor Garden, Inc. Due to Potential E....

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...

The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...

The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2020· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...

The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2020· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2020· Boddingtons Plastics Ltd

Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...

The Issue: Updated Instructions For Use- to contraindications and potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Skytron, Div. The KMW Group, Inc

Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...

The Issue: Intermittent failure of a signal being sent to a monitor from the touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...

The Issue: As part of an investigation into a biocompatibility test discrepancy where a...

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

Class II — Potential Health HazardOngoing