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. 2,524 recalls have been distributed to Montana in the last 12 months.
Showing 10381–10400 of 48,326 recalls
Recalled Item: Power-PRO 2 Recalled by Stryker Medical Division of Stryker Corporation Due...
The Issue: Cot may experience unintended motion due to damaged cables. Potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Par Formulations Private...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...
The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S5 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid q ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...
The Issue: Potential that insert will be unable to disengage from the vertebral body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid i N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Latanoprost (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx NJ...
The Issue: Subpotent Drug: The batches contain less than 90% of the labeled amount of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of assurance of sterility: Bags have the potential to leak in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ETEST CLINICAL AMIKACIN AK 256 US S30 Recalled by Biomerieux Inc Due to As...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PPM LOMBARD PRODUCTS TSA 10PLT Recalled by Biomerieux Inc Due to As the...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.