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. 1,071 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,071 in last 12 months

Showing 9041–9060 of 27,852 recalls

Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ear Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-4593AE) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· GE Healthcare, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer - Product Usage: Is a Recalled by...

The Issue: Image acquisition failures and synchronization failure with the Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is Recalled by...

The Issue: Image acquisition failures and synchronization failure with the Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Philips Ultrasound Inc

Recalled Item: Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0 Recalled by...

The Issue: Due to a software defect that can intermittently cause the system to lock-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Smiths Medical ASD Inc.

Recalled Item: NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129 Recalled by Smiths...

The Issue: There is potential for harmful levels of aluminum leaching when using lower...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-3893AE) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing