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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 19341–19360 of 27,254 recalls
Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated...
The Issue: Due to a packaging error; The kit does not contain the correct number of C1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...
The Issue: There are potential issues with results reporting for certain run-based...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage:...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product...
The Issue: A potential problem associated to the gradient coil (ASGC) in the Titan 3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium on RX Imola analyser IVD Recalled by Randox Laboratories, Limited...
The Issue: According to the firm, Carry over was observed when the amylase or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has identified changes in default carry forward workflow using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentaray NAV High-Density Mapping ECO Catheter Recalled by Biosense Webster,...
The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentaray NAV High-Density Mapping Catheter Recalled by Biosense Webster,...
The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient...
The Issue: Medtronic Respiratory & Monitoring Solutions Announces a Voluntary Recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera/Skyra Systems Recalled by Siemens Medical Solutions USA, Inc...
The Issue: The docking station top cover of the removable patient table may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglyceride Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uric Acid Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.