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. 2,251 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,251 in last 12 months

Showing 4504145060 of 46,762 recalls

Medical DeviceSeptember 13, 2012· 3M Company - Health Care Business

Recalled Item: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac...

The Issue: 3M determined that the electrical grounding mechanism for the Steri-Vac 5XL...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2012· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost with patient carriage Model: 712050 with serial...

The Issue: Hook does not securely hold the footplate in vertical position, causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Magnetom Skyra Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: When positioning the Flex Large 4 Coil (part No. 8625761) off-center in...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2012· Whole Foods Market

Recalled Item: Frescolina and Mitica brand Ricotta Salata cheeses were cut into wedges...

The Issue: Whole Foods Market announces that it is recalling ricotta salata sold in 21...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR Assay: Catalog Number: US: Recalled by Siemens...

The Issue: BR Assay for CA 27.29 Calibration Interval Change due quality control (QC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart XL M4735A Defibrillator/Monitors Recalled by Philips...

The Issue: HeartStart XL Defibrillator/Monitor (M4735A) used on a patient when AC power...

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

Class II — Potential Health HazardOngoing
DrugSeptember 10, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS Recalled by Vintage...

The Issue: Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 10, 2012· Forever Cheese Inc

Recalled Item: Marte brand Frescolina Ricotta Salata. Matured and packed by: Fattorie...

The Issue: Frescolina brand Ricotta Salata cheeses found positive for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 10, 2012· Invacare Corporation

Recalled Item: Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility...

The Issue: The potential exists for the wheel to rotate freely despite engagement of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: Recalled...

The Issue: Terumo Cardiovascular Systems (CVS) received two reports of the false back...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Polyaxial Screw...

The Issue: This action is being initiated following a detailed investigation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap...

The Issue: This action is being initiated following a detailed investigation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Instrumentation Industries Inc

Recalled Item: Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators...

The Issue: Firm initiated an update to Directions for Use necessitating replacement of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Optovue Inc.

Recalled Item: materials "RETINAL OCT Analysis and Interpretation Method" shipped with...

The Issue: Devices labeled for an intended use not included in the existing 510(k) or...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Baxter Healthcare Corp.

Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...

The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 7, 2012· Baxter Healthcare Corp.

Recalled Item: Baxter Interlink System Buretrol Solution Set Recalled by Baxter Healthcare...

The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 7, 2012· Baxter Healthcare Corp.

Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...

The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 7, 2012· Baxter Healthcare Corp.

Recalled Item: Baxter Interlink System Buretrol Solution Set with 150 mL Burette Recalled...

The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...

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

Class I — Serious Health HazardOngoing