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. 2,258 recalls have been distributed to Alaska in the last 12 months.
Showing 44121–44140 of 46,762 recalls
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CALCIUM GLUCONATE INJECTION Recalled by Fresenius Kabi USA LLC (FK USA) Due...
The Issue: Labeling: Missing label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Recalled...
The Issue: Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vistide (cidofovir) Injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: Particulate matter was found in some vials...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Suprax (cefixime for oral suspension) USP Recalled by Lupin Pharmaceuticals...
The Issue: Discoloration; Product may not meet specifications for color description...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus...
The Issue: During the course of product monitoring, Siemens became aware of a tolerance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic...
The Issue: Potential failure of the braking system that controls the O-arm Imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echelon Recalled by Hitachi Medical Systems America Inc Due to Hitachi...
The Issue: Hitachi discovered a software error that can occur when simultaneously...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring sets with VAMP Plus closed blood sampling system...
The Issue: The device is being recalled because the firm has received multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Recalled by QIAGEN...
The Issue: CMV RG PCR kits may contain a mixture of incorrect vials among the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Recalled by QIAGEN...
The Issue: CMV RG PCR kits may contain a mixture of incorrect vials among the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.