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 4142141440 of 48,326 recalls

Medical DeviceApril 16, 2014· Sakura Finetek USA Inc

Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...

The Issue: This Lot has variations in melting temperature.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Maquet Medical Systems USA

Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...

The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...

The Issue: Test Strips may report an inaccurately low INR result. Several patients had...

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

Class I — Serious Health HazardOngoing
DrugApril 15, 2014· Sung Soo Kim

Recalled Item: Super ARTHGOLD 500mg Recalled by Sung Soo Kim Due to Undeclared Indomethacin

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2014· P&L Developments, LLC

Recalled Item: Children's Triacting Night Time Cold & Cough with PE (diphenhydramine...

The Issue: Presence of Precipitate: Small amounts of diphenydramine and mannitol...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Brainlab AG

Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...

The Issue: When using a specific plan update workflow in combination with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...

The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...

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

Class I — Serious Health HazardOngoing
DrugApril 14, 2014· Fresenius Kabi USA LLC

Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...

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

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· Golden State Medical Supply Inc.

Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...

The Issue: Presence of Foreign Substance; some bottles may contain debris that was...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 14, 2014· P&L Developments, LLC

Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Phenylephrine component is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· Upsher Smith Laboratories, Inc.

Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...

The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...

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

Class III — Low RiskOngoing
Refund
FoodApril 14, 2014· Health Matters America Inc.

Recalled Item: Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE...

The Issue: Undeclared milk allergen

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 14, 2014· Health Matters America Inc.

Recalled Item: Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80%...

The Issue: Undeclared milk allergen

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Ivoclar Vivadent, Inc.

Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...

The Issue: A stock check revealed broken glass fibers between the connector and the...

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

Class II — Potential Health HazardOngoing