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. 2,512 recalls have been distributed to Alaska in the last 12 months.
Showing 7361–7380 of 46,762 recalls
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Recalled by...
The Issue: Over-the-needle, intravascular catheters may have needles that do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor with VAMP System Recalled by Edwards Lifesciences, LLC Due...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruWave with Vamp System Pressure monitoring set Recalled by Edwards...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor with Vamp System Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...
The Issue: Potential for damaged and frayed power connector plug with repeated bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...
The Issue: Progressa+ beds have the potential for static buildup from the casters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use...
The Issue: Subpotent: Failing Test Results for Epinephrine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2% Lidocaine HCl Injection Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: identified as glass.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: identified as glass.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1% Lidocaine HCl Injection Recalled by Pfizer Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: identified as glass.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine-phenylephrine 1%-1.5% 1mL Single Dose Vial Recalled by Pine...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefuroxime 4mg /0.4 mL (10 mg/mL) Recalled by Pine Pharmaceuticals, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin in Balanced Salt Solution 400 mcg/0.4 mL (100 mcg/0.1 Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium chloride Solution for Intravenous Injection Recalled by Pine...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl 4% ophthalmic solution Recalled by Pine Pharmaceuticals, LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.