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. 979 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
979 in last 12 months

Showing 24961–24980 of 48,326 recalls

Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
FoodJune 29, 2018· LL'S MAGNETIC CLAY INC

Recalled Item: Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal...

The Issue: The recalled dietary supplement has the potential to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 29, 2018· Sisel International Llc

Recalled Item: Sisel Recalled by Sisel International Llc Due to Firm is recalling SiselRipt...

The Issue: Firm is recalling SiselRipt due to the presence of an unapproved artificial...

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

Class III — Low RiskOngoing
Refund
FoodJune 28, 2018· Pinnacle Food Group, Llc

Recalled Item: Wish Bone House Italian Salad Dressing 15 oz. Recalled by Pinnacle Food...

The Issue: The recall was initiated after learning from a retail customer that a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 28, 2018· Datex-Ohmeda, Inc.

Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...

The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2018· PFIZER

Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...

The Issue: Microbial Contamination of Sterile Products: Product associated with reports...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2018· LUPIN SOMERSET

Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...

The Issue: Subpotent Drug and Failed Content Uniformity.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 (Stitching Patient Support) 712225 Recalled by Philips...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Elekta Instrument AB

Recalled Item: Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based...

The Issue: The margin tool in Leksell GammaPlan 11.1 systematically overestimates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Classic Recalled by Philips Medical Systems Gmbh, DMC Due to...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030 Recalled by Philips...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing