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. 1,822 recalls have been distributed to Montana in the last 12 months.
Showing 24541–24560 of 27,852 recalls
Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...
The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.0 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...
The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...
The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled by Steris...
The Issue: Customers indicated fluctuations in environmental conditions sites and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Veris MR Monitor units The system is intended to Recalled by Medrad...
The Issue: The main board, P/N 301641, installed in some Medrad Veris MR Monitor units...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M ESPE Imprint II Regular Body Recalled by 3M Company - Health Care...
The Issue: Specific lots of Imprint II and Paradigm impression material packs are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Propaq LT Series monitors. Model numbers 802LTAN Recalled by Welch Allyn...
The Issue: Welch Allyn will update Propaq 802 Series Vital Signs Monitor, models are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...
The Issue: Individual discs in the lot may not be sufficiently impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normative Data Template CD for use with the I-Portal devices. Used to...
The Issue: The data provided on the Normative Data Template CD for use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.