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. 2,359 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,359 in last 12 months

Showing 3192131940 of 48,326 recalls

FoodJuly 28, 2016· Gel Spice Co, Inc.

Recalled Item: 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by Gel Spice Co....

The Issue: Ground Turmeric may contain excess levels of lead.

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 27, 2016· Akorn, Inc.

Recalled Item: Desoximetasone Gel USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: product was out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
FoodJuly 26, 2016· La Torre Foods Usa, Inc.

Recalled Item: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz Recalled by La...

The Issue: Calcium caseinate is declared on the label, but milk is not listed.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Encore Medical, Lp

Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...

The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Philips Electronics North America Corporation

Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...

The Issue: If an affected Patient Monitor has been powered on continuously for several...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Microgenics Corporation

Recalled Item: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...

The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...

The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...

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

Class II — Potential Health HazardOngoing
FoodJuly 23, 2016· Arcobasso Foods

Recalled Item: Panera Bread Balsamic Vinaigrette Dressing Recalled by Arcobasso Foods Due...

The Issue: Consumer complaints of bulging bottles.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 22, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to A firmware...

The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800 Recalled by GE OEC Medical Systems, Inc Due to A firmware issue in...

The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Inovo, Inc

Recalled Item: INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen Recalled by...

The Issue: Device can fail during operation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Smith & Nephew, Inc.

Recalled Item: RENASYS Sterile Transparent Film and all the RENASYS Dressing kits Recalled...

The Issue: Sterility seal integrity failures on the Renasys Sterile Transparent Film

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

Class II — Potential Health HazardOngoing