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. 2,517 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,517 in last 12 months

Showing 63416360 of 46,762 recalls

Medical DeviceFebruary 12, 2024· ARROW INTERNATIONAL Inc.

Recalled Item: ARROW QuickFlash Radial Artery Catherization (wire Recalled by ARROW...

The Issue: Teleflex is initiating this voluntary recall for the above-mentioned...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2024· Sarnova HC, Llc

Recalled Item: Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a Recalled...

The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2024· Think Surgical, Inc.

Recalled Item: Assembly Recalled by Think Surgical, Inc. Due to There is a galling effect...

The Issue: There is a galling effect (cold-weld) caused by friction between the array...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2024· Stason Pharmaceuticals, Inc.

Recalled Item: Mercaptopurine Tablets Recalled by Stason Pharmaceuticals, Inc. Due to...

The Issue: Failed Dissolution Specifications: results slightly under spec at at 9-months.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 9, 2024· Apotex Corp.

Recalled Item: Fluticasone Propionate Nasal Spray USP 50mcg Recalled by Apotex Corp. Due to...

The Issue: CGMP Deviations: potential presence of Burkholderia cepacia complex

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2024· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by The Harvard Drug Group LLC dba...

The Issue: an out of specification result obtained during routine stability testing for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2024· Preat Corp

Recalled Item: Preat Nobel Active/Conical-compatible RP Titanium Blank Recalled by Preat...

The Issue: Due to a manufacturing issue, the screw seat location on the abutment...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2024· EYE COMFORT CARE LLC

Recalled Item: Brand Name: UNclog Eye Mask Product Name: UNclog Eye Mask Recalled by EYE...

The Issue: Due to a change in the safety clips for the heated eye masks, the wires to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2024· Beckman Coulter, Inc.

Recalled Item: Access Total T4 Recalled by Beckman Coulter, Inc. Due to Four lots of Access...

The Issue: Four lots of Access Total T4 reagent lots demonstrated imprecision outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2024· Landauer

Recalled Item: microStar Reader Recalled by Landauer Due to Permanent discontinuance of the...

The Issue: Permanent discontinuance of the microSTARii medical dosimetry system....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2024· Baxter Healthcare Corporation

Recalled Item: CLEARLINK Non-DEHP Solution Set Luer Lock Adapter Recalled by Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
FoodFebruary 7, 2024· Trader Joe's Company

Recalled Item: Trader Joe s Cilantro Salad Dressing (SKU 36420) Perishable Keep Recalled by...

The Issue: L. mono contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2024· Trader Joe's Company

Recalled Item: Trader Joe s Elote Chopped Salad Kit (SKU 74768) 11.94 oz. Recalled by...

The Issue: L. mono contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2024· Trader Joe's Company

Recalled Item: Trader Joe s Southwest Salad (SKU 56077) 9 oz. Recalled by Trader Joe's...

The Issue: L. mono contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 7, 2024· Life Technologies Corporation

Recalled Item: Torrent Suite Dx Software versions 5.14 and earlier used in Recalled by Life...

The Issue: Torrent Suite Dx Software versions 5.14 and earlier used in connection with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Beckman Coulter, Inc.

Recalled Item: Access Substrate Recalled by Beckman Coulter, Inc. Due to On 07 February...

The Issue: On 07 February 2024 Beckman Coulter made the decision to conduct a field...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: TENSIVE Conductive Adhesive Gel Recalled by Natus Neurology Inc Due to Natus...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: natus neurology Recalled by Natus Neurology Inc Due to Natus has become...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing