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. 2,000 recalls have been distributed to Alaska in the last 12 months.
Showing 3161–3180 of 27,254 recalls
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essentia MAJ Laparotomy Std Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bilateral Tubal Ligation Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand Pack Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Vascular Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPB-0.7 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.2-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PACEMAKER PACK Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaginal Delivery Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY TORCH MODULE BOX Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY 2.0 INSTRUMENT Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR Procedure Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasal Sinus Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Day Surgery General Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system Recalled by...
The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety Recalled...
The Issue: The syringes that were inadvertently shipped from the Distribution Center....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 Set AU Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.