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. 2,530 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,530 in last 12 months

Showing 77617780 of 48,326 recalls

DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM MIST 15% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 5% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 15% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 5% Solution Recalled by Dr. Berne's Whole Health...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2023· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Stability data...

The Issue: Stability data does not support expiry: Shelf-life of the impacted lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2023· Hua Da Trading, Inc. dba Wefun Inc.

Recalled Item: WEFUN Capsules 825 mg Recalled by Hua Da Trading, Inc. dba Wefun Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2023· Marlex Pharmaceuticals, Inc.

Recalled Item: Digoxin Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to Labeling:...

The Issue: Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2023· Marlex Pharmaceuticals, Inc.

Recalled Item: Digoxin Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to Labeling:...

The Issue: Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
DrugAugust 24, 2023· Baxter Healthcare Corporation

Recalled Item: Doxil (doxorubicin hydrochloride liposome injection) 50 mg in 25 mL (2...

The Issue: CGMP Deviations: Product was exposed to temperatures exceeding the labeled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2023· MICROVENTION INC.

Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...

The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2023· Inmar Supply Chain Solutions, LLC

Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...

The Issue: Various medical devices potentially exposed to rodent and rodent activity....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2023· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Full screen error message may occur on patient monitors with affected...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2023· Contract Pharmaceuticals Limited Canada

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Contract...

The Issue: Defective Container: slow leakage under the cap

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 23, 2023· Stryker Corporation

Recalled Item: Cinchlock SS Knotless Anchor Inserter Recalled by Stryker Corporation Due to...

The Issue: Expired Product distributed

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Knee insert...

The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Encore Medical, LP

Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...

The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2023· Apellis Pharmaceuticals, Inc.

Recalled Item: Apellis Injection Kit 29g Injection Needle -single use intended to Recalled...

The Issue: 19-gauge x 1" inch filter needles showed appearances of a small fraction of...

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

Class II — Potential Health HazardOngoing