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. 2,326 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,326 in last 12 months

Showing 3424134260 of 46,762 recalls

DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Tf Supplements

Recalled Item: RHINO 7 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Actavis...

The Issue: Failed Dissolution Specifications: Low Out-of-Specification results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Tf Supplements

Recalled Item: Rhino 7 Platinum 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 24, 2015· Pfizer Inc.

Recalled Item: Xanax (alprazolam) tablets Recalled by Pfizer Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2015· Airways Development LLC

Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....

The Issue: Airways Development LLC has received a complaint about a canister leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· Berchtold Corp.

Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...

The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2015· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...

The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...

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

Class II — Potential Health HazardOngoing
DrugSeptember 23, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Pink Bikini Strong Formula capsules Recalled by Lucy's Weight Loss (dba....

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 23, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Shorts on The Beach Golden Edition by Pink Bikini Recalled by Lucy's Weight...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 23, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Shorts on The Beach Strong Formula by Pink Bikini capsules Recalled by...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 22, 2015· Midway Importing, Inc

Recalled Item: Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets...

The Issue: Cross Contamination With Other Products: Potential cross-contamination of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: Eon 100 system included the following product numbers and Recalled by...

The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...

The Issue: Users can merge a device import file with an image study that already has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...

The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...

The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2015· ELITech Clinical Systems SAS

Recalled Item: Eon 300 system includes the following product numbers and Recalled by...

The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...

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

Class II — Potential Health HazardOngoing