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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 3812138140 of 48,326 recalls

Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2015· Microtek Medical Inc

Recalled Item: LASER RESISTANT WAND - STERILE Recalled by Microtek Medical Inc Due to This...

The Issue: This recall is being conducted because a cohesive band used to package the...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2015· Navinta LLC

Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Guiltless Gourmet Southwestern Veggie Burger 2.5oz 48 pieces Distributed by:...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Black Bean Burger 4.5 oz 40 pieces Net Wt. 11.25 Recalled by Cuisine...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Southwestern 4oz Veggie Burger 36 count Net Wt 9 lb. Recalled by Cuisine...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Chef's Line Black Bean Burger 36-4.25 oz Net Wt. 9 Recalled by Cuisine...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product...

The Issue: Fujifilm is conducting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a Recalled...

The Issue: Fujifilm is reporting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS ROC Crown Component 4UR (5/pk) Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Specialty MiniScope Mech. Set Size 18 Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Recalled by Specialty...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit Recalled by Specialty Appliance...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 Recalled by Specialty...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: HTM Mechanism Set Set 16 Recalled by Specialty Appliance Works, Inc. Due to...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Herbst Universal Nut which is used in a Herbst Appliance Recalled by...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Upper Right Telescope Unibodies (5/pk) and Upper Left Telescope Unibodies...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing