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. 1,043 recalls have been distributed to Montana in the last 12 months.
Showing 12701–12720 of 27,852 recalls
Recalled Item: JAPAN CELL SAVER ELITE SET - 225ML - Product Usage: Recalled by Haemonetics...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAPAN DISP SET Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Japan DISP SET Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxM 1040 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxM 1096 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...
The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...
The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Scenaria Whole-body X-ray CT System Recalled by Hitachi Medical...
The Issue: There is a possibility that the cables to the controller unit may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.