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 2521–2540 of 27,852 recalls
Recalled Item: StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog...
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683....
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216 Recalled by...
The Issue: The following four issues are included: 1. Certain Channel Settings may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE SAFELINK Recalled by Greiner Bio-One GmbH Due to The VACUETTE...
The Issue: The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT Recalled by...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) Port Access Kit Recalled by MEDLINE...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 6 Plus Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT and Spectral CT Plus. Model Numbers: 728333 Recalled by Philips...
The Issue: Potential for a plan box not updated issue during Interventional procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number:...
The Issue: The warming surfaces or incubator well temperatures of the listed products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number:...
The Issue: The warming surfaces or incubator well temperatures of the listed products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have...
The Issue: Some software versions have a malfunction where they may show incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have...
The Issue: Some software versions have a malfunction where they may show incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number:...
The Issue: The warming surfaces or incubator well temperatures of the listed products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.