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. 2,470 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,470 in last 12 months

Showing 1586115880 of 48,326 recalls

DrugJanuary 25, 2021· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2021· Goodman Food Products Texas Inc

Recalled Item: O Organics Plant Based Mushroom and Veggie Organic Burger Patties Recalled...

The Issue: Labeling error caused product to claim Gluten Free and Vegan when it...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2021· Wildtree Inc.

Recalled Item: "Wildtree***Leslies Chili Blend***Organic & Gluten Free***Net Wt. 3.7 oz....

The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 25, 2021· Wildtree Inc.

Recalled Item: "Wildtree***Taco Seasoning***Organic & Gluten Free***Net Wt. 8...

The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2021· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...

The Issue: The size indicated on the labeling on the outer packaging, on the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2021· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...

The Issue: The size indicated on the labeling on the outer packaging, on the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2021· Medline Industries Inc

Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...

The Issue: Product was compromised during shipment.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...

The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...

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

Class II — Potential Health HazardOngoing
DrugJanuary 22, 2021· Ascend Laboratories LLC

Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...

The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2021· Ascend Laboratories LLC

Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...

The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 22, 2021· Acist Medical Systems

Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...

The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...

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

Class I — Serious Health HazardOngoing
DrugJanuary 21, 2021· Stanley Specialty Pharmacy Compounding and Wellness Center

Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...

The Issue: Superpotent Drug. Lidocaine higher concentration than listed

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Oseltamivir Phosphate for Oral Suspension Recalled by Lupin Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications; Out-of-specification test...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 21, 2021· Door County Coffee & Tea Co., Inc.

Recalled Item: Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. Recalled by...

The Issue: Retail Box did not contain list of ingredients or allergen statement.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2021· G & H Wire Company

Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...

The Issue: The text on the patient pack is correct and the product itself remains...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2021· CooperSurgical, Inc.

Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...

The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...

The Issue: Product was distributed without receiving regulatory clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Merit Medical Systems, Inc.

Recalled Item: Heartspan Transseptal Needles Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Merit Medical Systems, Inc.

Recalled Item: HeartSpan Transseptal Needles Catalog No. FND-019-01 Recalled by Merit...

The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· ReNovo, Inc.

Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...

The Issue: Non-sterile product was shipped to customers labelled as sterile.

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

Class II — Potential Health HazardOngoing