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. 2,417 recalls have been distributed to Alaska in the last 12 months.
Showing 19421–19440 of 46,762 recalls
Recalled Item: Sidus Stem-Free Shoulder Humeral Head Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL Recalled by Zimmer Biomet, Inc....
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Recalled by Zimmer Biomet, Inc. Due...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fitmore Hip Stem Recalled by Zimmer Biomet, Inc. Due to Non-highly polished...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coorad Morrey Total Elbow Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Hip Joint Replacement Systems Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Devices Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB Proximal Lateral Tibia Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SM DIS VOL/DORS RAD LAT COL PLATE Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl Recalled by...
The Issue: Lack of Assurance of Sterility; bags have potential to leak
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Recalled by...
The Issue: GMP Deviations: potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Recalled by...
The Issue: GMP Deviations: potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: del Nido Cardioplegia Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility; bags have potential to leak
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Recalled by...
The Issue: GMP Deviations: potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leucovorin Calcium Injection Recalled by Ingenus Pharmaceuticals Llc Due to...
The Issue: Crystallization: Presence of particulate matter identified as API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability...
The Issue: Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo carry-on Procedure Kit - Product Usage: Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.