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. 2,283 recalls have been distributed to Alaska in the last 12 months.
Showing 42341–42360 of 46,762 recalls
Recalled Item: LeGoo Internal Vessel Occluder 1mL Product Number: 10-0100 LeGoo is Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo with 3 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder .5mL Product Number: 10-0050 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo with 3 Cannula Recalled by...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo w/ no Cannula Product...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.25 mL LeGoo with 3 Cannula Pouch...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MHI-TM2000 Linear Accelerator System Recalled by MITSUBISHI HEAVY...
The Issue: Software anomaly: Mitsubishi Heavy Industries, Ltd. became aware of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Picis ED Pulsecheck - EMR Software Application - 2125 Recalled by Picis Inc....
The Issue: Notes associated with prescription are not printed to the prescription or to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHENTALENE (TM) Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PHEnFX (TM) Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RED VIPERS Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxyphen XR Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...
The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...
The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.