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. 2,353 recalls have been distributed to Alaska in the last 12 months.
Showing 22501–22520 of 27,254 recalls
Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...
The Issue: Cardiohelp- i System may have a software issue that can potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Neg Urine Combo Panel Type 1 Recalled by Siemens Healthcare...
The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...
The Issue: Report received where the Align Radial Stem fractured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...
The Issue: The box of guides for a specific case arrived intact but contained two (2)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads...
The Issue: To provide clarifying instructions relating to the assembly/disassembly of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices. Models H3000YA Recalled by...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia (including Infinia Recalled by GE Healthcare, LLC Due...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo NM615 Recalled by GE Healthcare, LLC Due to GE is issuing this recall...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima NM/CT 640 Recalled by GE Healthcare, LLC Due to GE is issuing this...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging...
The Issue: GE is issuing this recall due to a potential safety issue related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE is updating the...
The Issue: GE is updating the Preventative Maintenance procedure and schedule, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Tibial Impactor Replacement Pads. Product Usage: TM Tibial...
The Issue: To provide clarifying instructions relating to the assembly/disassembly of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.