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. 2,277 recalls have been distributed to Montana in the last 12 months.
Showing 45361–45380 of 48,326 recalls
Recalled Item: Centricity Perinatal and Centricity Intensive Care is intended to be...
The Issue: 1) Under rare network conditions, a Centricity Perinatal process may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood. Used Recalled by...
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood and Recalled by Becton...
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms....
The Issue: Microbiological media may be contaminated with bacteria.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All OneTouch Verio IQ Blood Glucose Meters sold as: Verio Recalled by...
The Issue: The Verio IQ meter will shut off and revert to set up mode at glucose values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the Recalled by...
The Issue: Siemens has observed that the listed lot numbers show an increase in Heparin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metal cans Recalled by La Preferida Inc Due to Some cans may not have been...
The Issue: Some cans may not have been fully processed which could result in product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LifeCare PCA Infusion System with Hospira MedNet Software Recalled by...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA 3 Recalled by Hospira Inc. Due to Screw rotation error...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA Plus II infusion pump system is designed for safe Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 system cam be used in a wide range of clinical settings Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare Pump Model 4200 PCA Infuser makes possible the Recalled by...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA infusion system with Hospira MedNet software allows clinicians...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 Recalled by...
The Issue: Recall is being initiated due to the part being mislabeled (Part Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture Recalled by...
The Issue: A post market safety review following several customer complaints indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICYCL-E- Lite Portable Oxygen System An integrated portable oxygen...
The Issue: A number of MEDICYL-e Portable Oxygen Systems may have misapplied valve flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APLIF Implants and Instruments Recalled by Spinal Solutions, LLC Due to...
The Issue: Spinal Solutions is recalling the APLIF system because it is not supported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Recalled by...
The Issue: Ormco Corporation is voluntarily recalling one (1) lot of Bracket Buccal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Systems with Software Artis VC20x/VC21A/VD10x that have a DSA Recalled...
The Issue: The firm has become aware of a potential issue on Artis systems with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifadin Recalled by Sanofi US Due to Subpotent drug: low fill volume in some...
The Issue: Subpotent drug: low fill volume in some of the capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.