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. 2,348 recalls have been distributed to Alaska in the last 12 months.
Showing 25761–25780 of 46,762 recalls
Recalled Item: Bull Capsules Recalled by BYL Solutions Inc. Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from Morphine...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from Fentanyl...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile drug preparations remaining within expiry prepared from...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLUE PEARL capsules Recalled by Blue Fusion Natural Due to Undeclared Sildenafil
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by Prinston Pharmaceutical Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: confirmed customer complaint of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BCI Advisor Vital Signs Monitor Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Some printing modes on the devices may not function properly (tabular data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...
The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR SIZE 0 STD prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX GSF OPT SZ C-L¿ LPS-FLEX GSF OPT SZ C-R¿ Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM PRC LT M/RT L SML FEM PRC RT M/LT Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIPOLAR METAL SHELL 48 MM OD Use of the MultiPolar Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.