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. 1,836 recalls have been distributed to Montana in the last 12 months.
Showing 18421–18440 of 27,852 recalls
Recalled Item: Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DP450 Recalled by Hidrex GmbH Due to The device was reclassified...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-series lift - A625 Manual w/Load Cell & Wi-Fi Recalled by ErgoSafe...
The Issue: During internal cycle test at max load (625 lbs.) 2 units had straps break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage:...
The Issue: Maquet has received several complaints involving the VASOVIEW HEMOPRO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg...
The Issue: After a receiving a customer complaint for incorrect labeling, BD has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 Flex Model #: 393-090 Portable Recalled by Radiometer America Inc Due...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to...
The Issue: Customer reports of the device handset continuing to operate after release...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL800 Model#:All Recalled by Radiometer America Inc Due to Reports that...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...
The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS HI and Mevatron M2/Primus Mid-Energy Recalled by Siemens Medical...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6730/6740 (MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON MD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm...
The Issue: The firm received one complaint from one non-US sales representative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON KD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...
The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) Recalled...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Drape Recalled by Covidien LLC Due to Sterility compromised...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.