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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 26481–26500 of 27,254 recalls
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith &...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian ARIA Oncology Information System Recalled by Varian...
The Issue: A software anomaly has been identified with the Import Export Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPIDER Surgical Instrument: Flexible Clip Applier The SPIDER¿ Surgical...
The Issue: Some clip applier units may be inadequate to achieve clip closure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Blanket Protective Coverlet Recalled by Beekley Corporation Due to...
The Issue: Imaging artifact can occur on mammogram result
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL 9NC Coagulation Sodium Citrate 3.2% Recalled by Greiner Bio-One North...
The Issue: Part of the lot received a lower concentration of citrate solution which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Philips Healthcare was notified that several of the sixteen bolts securing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc....
The Issue: A routine internal quality check found that the Drager PT 4000 Phototherapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge HEMO software. Recalled by Merge Healthcare, Inc. Due to The...
The Issue: The International Normalized Ratio (INR) value displayed in the study report...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY LIQUIBEADS Vaginal Moisturizer Recalled by Mc-NEIL-PPC, Inc. Due to...
The Issue: Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix...
The Issue: Ethicon and Omrix Biopharmaceuticals have received reports of air or gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Foley procedural trays packaged in breather bags. The product Recalled...
The Issue: Incomplete seal on sterile packages of product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS 7-color Setup beads BD Biosciences Recalled by BD Biosciences,...
The Issue: Incorrect version of the CD was included with BD FACS 7 Color Setup Beads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Encore Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chorus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sara Plus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due...
The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module model 8100. Subsequent product code: FPA The Recalled by...
The Issue: The recall was initiated because Carefusion identified a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DGXN Slides --- [REF] 834 3386. Product Recalled...
The Issue: Ortho Clinical Diagnostics revised the VITROS Chemistry Products DGXN Slides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD Cyclesure Biological Indicator (BI) Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling certain lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
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: Mar Cor Purification CWP Reverse Osmosis System. Models 101 Recalled by Mar...
The Issue: There exists a potential situation with the crimp connection at the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.