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. 2,353 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,353 in last 12 months

Showing 2440124420 of 46,762 recalls

DrugJune 4, 2018· HOSPIRA INC, LAKE FOREST

Recalled Item: Naloxone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST Due to...

The Issue: Presence of Particulate Matter; Potential for particulate matter on the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 4, 2018· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Suction Irrigator Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The firm has identified the potential for a silicone particle to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Fx Solutions

Recalled Item: Fx SOLUTIONS CENTERED HEAD CoCr 50x19 Recalled by Fx Solutions Due to Breach...

The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Leica Microsystems, Inc.

Recalled Item: Leica Microsystems products labeled as the following: Leica M320 Microscope...

The Issue: Possible failure of screws which hold the gas spring fixation bracket in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Neomed Inc

Recalled Item: NeoMed Enteral Feeding Tubes with Enteral Only Connectors Recalled by Neomed...

The Issue: Potential for the tethered plug on the hub of the NeoMed Enteral Feeding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Fx Solutions

Recalled Item: Fx SOLUTIONS OFFSET HEAD CoCr 50x20 Recalled by Fx Solutions Due to Breach...

The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Richard-Allan Scientific Company

Recalled Item: EZ Single Cytofunnel Brown Recalled by Richard-Allan Scientific Company Due...

The Issue: Mislabeled product

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

Class III — Low RiskOngoing
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.45% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· Apotex Inc.

Recalled Item: Fluticasone propionate Nasal Spray Recalled by Apotex Inc. Due to Presence...

The Issue: Presence of foreign substance: glass particles

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of assurance...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Presence of Foreign Substance: A product complaint was received for a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2018· Baxter Healthcare Corporation

Recalled Item: FLOSEAL Special Applicator Tips in cartons labeled in part Recalled by...

The Issue: Baxter r recalled this device due to the use of an incorrect plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2018· Zeiss, Carl Inc

Recalled Item: Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope...

The Issue: Under certain circumstances, the firmware makes it possible for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile Recalled...

The Issue: Cap may be mislabeled with incorrect part number, although the correct part...

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

Class II — Potential Health HazardOngoing
DrugMay 29, 2018· Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...

The Issue: Resuspension problems: Out of specification for appearance and resuspendability.

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

Class III — Low RiskOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund