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. 2,384 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,384 in last 12 months

Showing 2014120160 of 46,762 recalls

Medical DeviceJuly 18, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas 8000 Modular Analyzer Series: cobas 8000 ISE module part Recalled by...

The Issue: Quality issue with high pressure solenoid valves

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...

The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c513 Analyzer Recalled by Roche Diagnostics Operations, Inc. Due to...

The Issue: Quality issue with high pressure solenoid valves

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Medical Intelligence Medizintechnik Gmbh

Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...

The Issue: Sometimes, although the HexaPOD has reached the target position, the...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream USP100 Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out-of-specification result...

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

Class III — Low RiskOngoing
Refund
DrugJuly 17, 2019· Macleods Pharma Usa Inc

Recalled Item: Tamsulosin Hydrochloride Capsules Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Bionpharma Inc.

Recalled Item: Clobazam Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Out-of-specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 16, 2019· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The...

The Issue: Non-conforming devices are identified, which may not have been included in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· Philips North America, LLC

Recalled Item: Philips Azurion systems with software version R1.2 -Interventional...

The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2019· The Crystal Spoon Corp.

Recalled Item: Top Chef Meals Grilled Bison Burger best used by date Recalled by The...

The Issue: Product may be contaminated with E.coli

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 16, 2019· Jelly Belly

Recalled Item: Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g) Recalled by Jelly Belly...

The Issue: Confectionary bag states Gluten Free, while the ingredient statement lists...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 16, 2019· TeDan Surgical Innovations LLC

Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: There was incorrect raw material used in the production of the identified lot.

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

Class II — Potential Health HazardOngoing