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. 2,443 recalls have been distributed to Montana in the last 12 months.
Showing 19421–19440 of 48,326 recalls
Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HardyCHROM MRSA Recalled by Hardy Diagnostics Due to False Positive results...
The Issue: False Positive results due to the MSSA (methicillin-susceptible) strain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Xtra Blood Glucose & Ketone Monitoring System Recalled by Abbott...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optium EZ Blood Glucose Monitoring System Recalled by Abbott Diabetes Care,...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Precision H Blood Glucose and Ketone Monitoring System Recalled by...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranitidine Oral Solution Recalled by Precision Dose Inc. Due to CGMP...
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Silver Bullet Recalled by Natures Rx Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eleganza 5 (AC powered adjustable bed) Recalled by Linet Spol. S.r.o. Due to...
The Issue: A component used within the side rail mechanism may malfunction, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion...
The Issue: Sterile barrier system may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fentaNYL 1000 mcg/20 mL (50 mcg/mL) 20 mL in 20 mL Syringe Preservative Free...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 250 mcg/5 mL (50 mcg/mL) Recalled by QuVa Pharma, Inc. Due to...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2500 mcg/250 mL (10 mcg/mL) in 0.9% Sodium Chloride Recalled by...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2000 mcg/100 mL (20 mcg/mL) in 0.9% Sodium Chloride Recalled by...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2750 mcg/55 mL (50 mcg/mL) 55 mL Syringe Recalled by QuVa Pharma,...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.