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. 2,534 recalls have been distributed to Alaska in the last 12 months.
Showing 3701–3720 of 27,254 recalls
Recalled Item: Bag Decanter II Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vial Decanter Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bottle Decanter Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flow Bag Decanter Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transfer Device Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...
The Issue: Heater shaker module does not perform heating if the temperature is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTLR190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Non-Sterile Flyte hood covers the user s head and Recalled by Stryker...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurostimulation Kit (Ported Recalled by Nalu Medical, Inc. Due to...
The Issue: Neurostimulation Systems have a manufacturing non-conformance that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This product is a single use sterile device that is Recalled by Stryker...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Recalled by Stryker Corporation Due to Expired Products distributed...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Kittner Blunt Dissecting Instrument Recalled by ASPEN SURGICAL...
The Issue: The affected products may have been packaged with a defect in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nanoplasty 3D Bunion Correction System Implant Recalled by Treace Medical...
The Issue: Potential issue causing a higher frequency of interference with locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.