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 70417060 of 46,762 recalls

DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%) Recalled by Kilitch...

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 (Propylene glycol 0.6%) Recalled by...

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
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: 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: Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium 1%) Recalled by...

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: Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by Kilitch...

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: Lubricant Gel Drops (Polyethylene glycol 400 0.4% Recalled by Kilitch...

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: Lubricant Gel Drops (Carboxymethylcellulose sodium 1.0%) Recalled by Kilitch...

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 Dry Eye Relief (Polyethylene glycol 400 0.4% and Recalled by...

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: Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by Kilitch Healthcare...

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· KINDER FARMS LLC

Recalled Item: KinderMed INFANTS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2023· KINDER FARMS LLC

Recalled Item: KinderMed KIDS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
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· 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· 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 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Fagron Compounding Services

Recalled Item: Tropicamide 1% (10mg/mL) Recalled by Fagron Compounding Services Due to...

The Issue: Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the...

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

Class III — Low RiskOngoing
Refund