Atlas FDA

HENRY SCHEIN(R) 100-8008 Explorer-Double End #5. Barcode *+H658100800808*. Made in China. For professional use only. Ins

FDA device recall Z-0834-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Hu-Friedy Mfg Co, Inc.
Reason for recall
Reports of breakage on some dental explorers were received by the own label distributor and forwarded to Hu-Friedy Mfg. Co. (importer of record & Spec. Setter). Investigation conducted by Hu-Friedy Mfg. Co. revealed that the tips of the instruments may have been improperly heat treated and have the potential for unexpected tip fracture.
Action taken
On 3/29/04, Hu-Friedy Mfg. Co. notified Henry Schein, Inc. of the recall by telephone. This was followed up with a letter on 4/2/04. Henry Schein initiated a sub-recall to its customers by sending recall letters and response forms (dated 3/31/04) by First Class Mail on 4/2/04 & 4/5/04. The mailing will be followed up with fax, e-mail or phone calls.
Root cause
Other
Status
Terminated
Product code
EKB
Distribution
The products were sold to the sole direct account: the Own Label Distributor, Henry Schein, Inc. in Melville, NY. Henry Schein further distributed the explorers to end users nationwide and internation
Date initiated
2004-03-29
Date posted
2004-07-20
Date terminated
2012-08-02
Location
Chicago, IL

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