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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 4088140900 of 48,326 recalls

Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500...

The Issue: RAPIDPoint 500 Measurement Cartridges may have an error code one or more...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
FoodMay 23, 2014· Brunkow Cheese of Wisconsin, Inc.

Recalled Item: Fayette Creamery Jalapeno Pepper Raw Milk Cheddar Cold Pack Cheese Recalled...

The Issue: 8 oz tubs of Fayette Creamery brand Jalapeno Raw Milk Cheddar Cold Pack...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2014· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Metoprolol Succinate Extended Release Tablets Recalled by Dr....

The Issue: Failed Dissolution Specifications: Failure of dissolution test observed at...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2014· Sandoz, Inc

Recalled Item: Cefpodoxime Proxetil Tablets Recalled by Sandoz, Inc Due to Presence of...

The Issue: Presence of Foreign Substance: Presence of stainless steel particles.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2014· Aidarex Pharmaceuticals LLC

Recalled Item: Ciprofloxacin 500 mg tablets Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Presence of Foreign Tablets/Capsules: Tramodol 50 mg tablet has been found...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Barrel Bur Sterile Recalled by Stryker Instruments Div. of...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Philips Medical Systems, Inc.

Recalled Item: IntelliVue MX40 Wearable Patient Monitor in use with the Philips Recalled by...

The Issue: IntelliVue MX40 (part numbers 865350, 865352) with software revisions B.00...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 1.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Lindemann Drill Short Recalled by Stryker Instruments Div. of Stryker...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 6.0mm Round Fluted Bur Sterile Product Usage: The devices Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Barrel Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.0mm x 3.8mm Neuro Drill Soft Touch Sterile Product Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing