C2244.4308 CONELOG Titanium Base CC 4.3GH2 0.8 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutmen
FDA device recall Z-2205-2013 · posted 2013-09-16 · Terminated
Recall details
- Recalling firm
- Camlog Usa
- Reason for recall
- Product not cleared for sale/use in the United States.
- Action taken
- Camlog Usa notified four US consignees of the recall by telephone on August 5, 2013. The notification identified the recalled product, which did not have proper marketing clearance for distribution in the United States and asked customers to return all unused product. Cusotmers were sent an overnight UPS label via e-mail and asked customers to return the device to CAM:LOG USA Attn: Debby Callahan, 1822 Aston Avenue Carlsbad, CA 92007.
- Root cause
- No Marketing Application
- Status
- Terminated
- Product code
- NHA
- Quantity affected
- 6 to US customers
- Distribution
- USA Distribution in the states of NH, MD, CO, and IL.
- Date initiated
- 2013-08-28
- Date posted
- 2013-09-16
- Date terminated
- 2014-01-29
- Location
- Indianapolis, IN
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