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. 987 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
987 in last 12 months

Showing 18521–18540 of 46,762 recalls

Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 6MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 3MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN¿ BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 4MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 6MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 3MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 3MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 7.5MM(P) X 4MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 6MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 4MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 7.5MM(P) X 4MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 3MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 3MM(H)...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 4MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 6MM(H) Recalled...

The Issue: Resulting impression or scanned data produced from the Healing Abutment lots...

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

Class II — Potential Health HazardOngoing
DrugJanuary 10, 2020· Advanced Accelerator Applications USA, Inc.

Recalled Item: NETSPOT Recalled by Advanced Accelerator Applications USA, Inc. Due to...

The Issue: Defective Container: loose aluminum cap crimp for the dilution buffer vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Tri-Lo-Marzia (Norgestimate and Ethinyl Estradiol Tablets Recalled by Lupin...

The Issue: CGMP Deviations: Out of specification test result observed during...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 9, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...

The Issue: The products are being recalled due to reports of breakage broke at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...

The Issue: The products are being recalled due to reports of breakage broke at the...

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

Class II — Potential Health HazardOngoing