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.
Showing 45301–45320 of 46,762 recalls
Recalled Item: Instrumentation Laboratory ACL TOP 700 PN 0000280010 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP (Base) PN 0000280000 ACL TOP is Recalled...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crispy Punjabi Cookies Recalled by Deep Foods Inc Due to This recall has...
The Issue: This recall has been initiated due to Non-Declared Milk. This product may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test...
The Issue: Customers were not following the labeled assay procedure. This was due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...
The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...
The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Chemical Contamination: The product is being recalled due to complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Chemical Contamination: The product is being recalled due to complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Chemical Contamination: The product is being recalled due to complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...
The Issue: The firm initiated a recall after complaint investigations revealed that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...
The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...
The Issue: Respironics is recalling the V60 ventilator because certain blower motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...
The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...
The Issue: Firm has confirmed highter imprecision with the recalled lots on Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg)...
The Issue: Presence of Particulate Matter: One lot of Bacteriostatic Water for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.