FDA Recall Open, Classified

Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 burs/package, Rx.

Recall: Z-1008-2024 · Initiated January 11, 2024

Recall

Recall Number
Z-1008-2024
Event Number
93809
Firm
Brasseler USA I Lp
FEI Number
1032227
Product Code
EJL
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
January 11, 2024
Posted
February 7, 2024
Address
1 Brasseler Blvd, Savannah, GA, 31419-9576

Description

Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 burs/package, Rx.

Reason

The device has a grip detail (right angle latch) out of specification causing the bur to not adequately latch in the handpiece.

Action

The recalling firm issued letters dated 1/8/2024 on 1/11/2024 via certified mail. The letter explains the reason for recall and required customer actions. The actions included that upon receipt of the letter, confirm the quantity of unused recalled product in their inventory and set it aside for return. Return information will be emailed to the consignee with a return label. The Customer Service emailed the letters to consignees on 1/12/2024 and sent product return instructions in the email. Phone calls will be made on 1/16/2024 if no response if received from the consignee via email. The recalling firm will be recording the amount of product to be returned on the phone log which will be completed for every consignee contacted. During the call, the consignees will also be given the product return instructions.

Distribution

Worldwide - US Nationwide distribution in the states of AL, CA, CO, DC, IL, NY, OH, OR, PA, TN, TX, and WA. The country of Canada.

Quantity

440 burs