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. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 4066140680 of 46,762 recalls

Medical DeviceDecember 26, 2013· Vital Signs Colorado Inc.

Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...

The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...

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

Class II — Potential Health HazardOngoing
DrugDecember 23, 2013· Hospira Inc.

Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter- Confimed customer complaint of particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2013· Watson Laboratories Inc

Recalled Item: Carisoprodol Tablets Recalled by Watson Laboratories Inc Due to Presence of...

The Issue: Presence of Foreign Substance; metal particulates were visually observed in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 23, 2013· Mckesson Information Solutions LLC

Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...

The Issue: Images may be archived to an incorrect or invalid archive location resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...

The Issue: The locking mechanism that is intended to hold the control panel in a fixed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...

The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...

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

Class II — Potential Health HazardOngoing
DrugDecember 20, 2013· Carefusion 2200 Inc

Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15%...

The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Carefusion 2200 Inc

Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9%...

The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Watson Laboratories, Inc.-(Actavis) - Florida

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specifications: Split tablets were found in the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Perrigo Diabetes Care

Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...

The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...

The Issue: There is a potential for communication loss associated with the F5-01 Frame...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Zeiss, Carl Inc

Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...

The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Optimedica Corporation

Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...

The Issue: Potential for unexpected heating of the transformer mounting bolt located...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: MINERAL IV Injection Recalled by Abrams Royal Pharamacy Due to...

The Issue: Non-Sterility; analytical results found product to contain Sphingomonas...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Steris Corporation

Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that the outer shipping package for one lot (Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...

The Issue: Three problems were reported to the firm: When positioning for a relative...

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

Class II — Potential Health HazardOngoing