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. 1,882 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,882 in last 12 months

Showing 70217040 of 46,762 recalls

Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE kits and trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ARTERIAL BUNDLE NO CATHETER Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE BRONCHOSCOPY TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP is recalling certain kits and trays that were...

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

Class I — Serious Health HazardOngoing
FoodNovember 15, 2023· Raw Seafoods Inc.

Recalled Item: Frozen Recalled by Raw Seafoods Inc. Due to Undeclared Sesame

The Issue: Contains undeclared sesame seeds and milk

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 14, 2023· Baxter Healthcare Corporation

Recalled Item: Ondansetron Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Failed pH Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide...

The Issue: CARDIOHELP-i System was not properly tested to measure leakage current

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

Class III — Low RiskOngoing
Medical DeviceNovember 13, 2023· Steris Corporation

Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...

The Issue: Identification label on affected hookups could become illegible over time...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...

The Issue: There have been transcription errors on the Instructions For Use (IFU) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Blue Belt Technologies, Inc

Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...

The Issue: Possibility that the user is unable to resolve drill disconnection error...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2023· Maquet Medical Systems USA

Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...

The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...

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

Class II — Potential Health HazardOngoing
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Target brand High Performance Lubricant Eye Drops (Polyethylene glycol 400...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: CVS Health brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%)...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Velocity Pharma brand Lubricating Eye Drop (Propylene glycol Eye Drops 0.6%)...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%)...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: CVS Health brand Recalled by Kilitch Healthcare India Limited Due to...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund