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. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 3054130560 of 46,762 recalls

DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Moxifloxacin 1 mg/mL in Sterile Balanced Salt Solution (BSS) Intravitreal...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Placebo for Prednisolone Acetate 1% Recalled by Leiter's Compounding Due to...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Lidocaine HCl 1% - Phenylephrine HCl 1.5% in Sterile Water Recalled by...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Cefuroxime Sodium 10 mg/mL in 0.9% Sodium Chloride (Injection) 1 Recalled by...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Bausch & Lomb Inc Irb

Recalled Item: PeroxiClear Peroxide Solution Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Product was found to contain excess residual levels of hydrogen peroxide.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Encore Medical, Lp

Recalled Item: Empowr PS Knee System Box Cut Guide The EMPOWER PS Recalled by Encore...

The Issue: It has been discovered that during Empowr PS Total Knee replacement, while...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...

The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...

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

Class II — Potential Health HazardOngoing
FoodSeptember 17, 2016· Mccormick

Recalled Item: Club Size McCormick Original Taco Seasoning Mix 24 oz. Recalled by Mccormick...

The Issue: Product was recalled due to undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: National Foods Packaging Low Sodium Chicken Base in 50 lb Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 16, 2016· Natus Medical Incorporated

Recalled Item: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...

The Issue: The firm sent the Technical Bulletin to consignees who received the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing