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. 2,353 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,353 in last 12 months

Showing 2492124940 of 46,762 recalls

Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E95 ultrasound system Product The device is intended Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid 7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2018· Mayne Pharma Inc

Recalled Item: Fabior (tazarotene) Foam Recalled by Mayne Pharma Inc Due to Superpotent...

The Issue: Superpotent Drug: High out of specification results for tazarotene assay at...

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

Class III — Low RiskOngoing
Refund
FoodMarch 21, 2018· Swire Coca Cola USA

Recalled Item: Dr. Pepper Est. 1885 Diet Recalled by Swire Coca Cola USA Due to Foreign...

The Issue: Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 21, 2018· Poppies International INC

Recalled Item: GFS Belgian Mini Chocolate Topped Eclairs Recalled by Poppies International...

The Issue: Products may be contaminated with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
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· 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· 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 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· 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· 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· 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