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. 1,645 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,645 in last 12 months

Showing 4562145640 of 46,762 recalls

FoodJune 21, 2012· J F C International Inc

Recalled Item: Tablemark Kaki (Oyster) Fry Recalled by J F C International Inc Due to JFC...

The Issue: JFC International Inc. is recalling Oyster IQF L size Frozen wild, PAFCO...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2012· J F C International Inc

Recalled Item: Breaded Oyster Frozen Recalled by J F C International Inc Due to JFC...

The Issue: JFC International Inc. is recalling Oyster IQF L size Frozen wild, PAFCO...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2012· J F C International Inc

Recalled Item: PAFCO Oyster Meat Tiny IQF Recalled by J F C International Inc Due to JFC...

The Issue: JFC International Inc. is recalling Oyster IQF L size Frozen wild, PAFCO...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2012· J F C International Inc

Recalled Item: Pacific Surf Breaded Oyster Fry Recalled by J F C International Inc Due to...

The Issue: JFC International Inc. is recalling Oyster IQF L size Frozen wild, PAFCO...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza Radiological Image Processing System Usage: Radiological...

The Issue: Firm has become aware of an unintended behavior when using syngo.plaza and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 8000 Base Product Usage: The Sarns Modular Perfusion System Recalled...

The Issue: During a retrospective review of complaint events, TCVS identified on...

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

Class III — Low RiskOngoing
Medical DeviceJune 20, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A Recalled by...

The Issue: HeartStart MRx Unexpected Pads/Paddles ECG Failure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Gulf South Medical Supply Inc

Recalled Item: Select Medical Products Vinyl Powder-Free Exam Gloves Recalled by Gulf South...

The Issue: Gulf South Medical Supply recalled their Select Medium and Large size Vinyl...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A...

The Issue: Therapy Cable Connection wear may lead to a malfunction in detection of...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2012· Medtech Products, Inc.

Recalled Item: Little Remedies For Tummys Recalled by Medtech Products, Inc. Due to...

The Issue: Subpotent (Single Ingredient) Drug: This product is being recalled because...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2012· Eos Imaging Inc

Recalled Item: EOS X-ray Medical Diagnostic Recalled by Eos Imaging Inc Due to It was...

The Issue: It was discovered of several generator failures of the EOS System due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2012· Advanced Sterilization Products

Recalled Item: STERRAD 100S Cassette Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...

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

Class III — Low RiskOngoing
Medical DeviceJune 19, 2012· Advanced Sterilization Products

Recalled Item: STERRAD NX Cassette Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...

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

Class III — Low RiskOngoing
Medical DeviceJune 19, 2012· Stryker Endoscopy

Recalled Item: Stryker brand Arthroscope and Hardware Set Tray (sterilization tray)...

The Issue: The gravity steam, Ethylene Oxide (EO) and STERRAD 100S sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2012· CareFusion 203, Inc.

Recalled Item: CareFusion EnVe Ventilator Designed for use on patients who require Recalled...

The Issue: CareFusion identified that the EnVe Ventilator may not hold the set Positive...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 100/120V. The Recalled by...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Cardiovascular Systems, Inc.

Recalled Item: CSI Stealth 360-degree Orbital Atherectomy Device (OAD) Recalled by...

The Issue: CSI has initiated a recall on specific lot numbers of Stealth 360-degree...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Synthes USA HQ, Inc.

Recalled Item: MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS)...

The Issue: Synthes is initiating a Medical Device Labeling Correction following a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing