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.
Showing 40741–40760 of 48,326 recalls
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...
The Issue: Failed Dissolution Specifications: Stability results found the product did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer-250 [succinic acid (from 250 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer [succinic acid (from 100 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...
The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...
The Issue: A small number of sealed foil pouches containing the electrodes were found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...
The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...
The Issue: Two lots of screws were commingled. Screws with etching and machining for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...
The Issue: Loosened monitor arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For...
The Issue: Potential for misalignment of the Z-stage scale. Using one of these devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...
The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritium Sternal Plate System Recalled by PIONEER SURGICAL TECHNOLOGY, INC....
The Issue: Lack of Sterility Assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ LED Battery Charger Recalled by Integra LifeSciences Corp. Due to...
The Issue: LED battery chargers may prematurely fail and will not charge the LED...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O....
The Issue: ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX 1200 Compounder Recalled by Baxter Healthcare Corp. Due to If the...
The Issue: If the universal ingredient (UI) in an active configuration is changed using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to Laser...
The Issue: Laser aperture label was not affixed to device prior to shipment in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coat-A-Count Direct Androstenedione Recalled by Siemens Healthcare...
The Issue: The assay is demonstrating a higher frequency of results greater than 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Auto-reader. Model numbers 390 Recalled by 3M Company - Health...
The Issue: Labeling on units shipped prior to May 16th, 2014 did not contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DENBLAN Anticavity Fluoride Toothpaste Recalled by Estee Lauder Inc Due to...
The Issue: Stability Data Does Not Support Expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.