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. 2,443 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,443 in last 12 months

Showing 1918119200 of 48,326 recalls

Medical DeviceDecember 20, 2019· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...

The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodDecember 19, 2019· Whole Foods Market

Recalled Item: 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes Recalled...

The Issue: Potential to contain undeclared milk and coconut.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Whole Foods Market

Recalled Item: 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes Net Wt Recalled...

The Issue: Potential to contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Randox Laboratories, Limited

Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...

The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...

The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Zimmer Biomet, Inc.

Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...

The Issue: Potential issue associated with the instrument -end of the shaft could fail...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Enzymatic Creatinine (ECREA) reagent Recalled by Siemens...

The Issue: There is a potential for falsely depressed creatinine results for patients...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 4/0 30 VIO SC-2 124K Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23 Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 3/0 30 VIOLET GS-11 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing