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. 1,071 recalls have been distributed to Montana in the last 12 months.
Showing 8261–8280 of 48,326 recalls
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion FMS Pak Recalled by Alcon Research, LTD. Due to Reports of patient...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Neuro Match Head Recalled by Stryker Corporation Due to There...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Precision Neuro Match Head Recalled by Stryker Corporation Due...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is Recalled by...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Cipla USA, Inc. Due to...
The Issue: Defective container: empty inhaler and leakage observed through the inhaler...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tizanidine Hydrochloride Tablet 4mg Recalled by Preferred Pharmaceuticals,...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Strides Pharma Inc. Due to Presence...
The Issue: Presence of Foreign Substance: Presence of a small piece of blue plastic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fargo Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISee Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YAMATO PLUS IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes and Surgical Room Turnover (SRT) Kits: Recalled...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellacor System with Micro-Coring Technology-Indicated for use by medical...
The Issue: Potential failure of a bearing adhesive joint that can occur due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 8Fr. IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANS-RAY IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 7.5Fr IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION 7 Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REINFORCED INTRODUCER SET Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift Visual Obturator Recalled by Scholly Fiberoptic Gmbh Due to There is...
The Issue: There is an improperly performed weld between the cone of the sheath lock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.