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. 2,568 recalls have been distributed to Montana in the last 12 months.
Showing 1901–1920 of 27,852 recalls
Recalled Item: Atellica CH Revised C Reactive Protein (RCRP) Recalled by Siemens Healthcare...
The Issue: Incorrect software flagging may occur for the assay that may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower Recalled by CareFusion...
The Issue: Due to a software bug, automated dispensing cabinet is unable to calculate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK (Name Recalled by CareFusion 303, Inc. Due to Users trying...
The Issue: Users trying to restock a single bin location of an automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...
The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...
The Issue: Nerve Monitoring System with certain software versions has potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...
The Issue: The devices are missing the laser marked depth markings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT...
The Issue: AutoPulse NXT Resuscitation System may not provide adequate chest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimulation RC Clinician Programmer Application Recalled by Medtronic...
The Issue: There is a software issue that can permanently disable communication with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.