Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,440 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,440 in last 12 months

Showing 1562115640 of 27,254 recalls

Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad with 4" Button Brush Recalled by Madison...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ MULTI 1 SDIL Recalled by Siemens Healthcare Diagnostics,...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ MULTI 2 SDIL Recalled by Siemens Healthcare Diagnostics,...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: Draco Enzymatic Deep-Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: Travel Kit Recalled by Madison Polymeric Engineering Due to The products...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ CTNI Sample Diluent Recalled by Siemens Healthcare...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Certified Safety Mfg Inc

Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...

The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2018· Synthes, Inc.

Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...

The Issue: There is a potential for the connection screw of the stem extractor to break.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Nobel Biocare Usa Llc

Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...

The Issue: The product label has missing information, such as the lot number and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: ACS-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing