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. 2,359 recalls have been distributed to Montana in the last 12 months.
Showing 29461–29480 of 48,326 recalls
Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...
The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zinc Oxide Paste 25% Recalled by Fagron, Inc Due to Labeling: Error on...
The Issue: Labeling: Error on Declared Strength: Error is due to an incorrect value in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief Diphenhydramine HCl 25 mg Recalled by P & L Development, LLC...
The Issue: Subpotent: This product is being recalled due to low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...
The Issue: nail not properly engaging with the targeting jig due to certain undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...
The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol (17-B-Estradiol Recalled by Spectrum Laboratory Products, Inc. Due...
The Issue: CGMP Deviations: these repackaged and redistributed products are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...
The Issue: CGMP Deviations: these repackaged and redistributed products are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS Recalled by...
The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...
The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...
The Issue: An unexpected transient mode switch behavior was detected by Medtronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...
The Issue: An extremely dusty computer can cause problems at system start, or rarely,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...
The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...
The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI . The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.