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FDA Medical Device Recalls (openFDA)

Telefelx Medical: Weck, DuraHook", Catalog #382800, 1/4" (6mm) Neuro Elastic Retractors, Sterile, Rx only.

Recall number
Z-1856-2008
Recalling firm
Telefelx Medical
Product
Weck, DuraHook", Catalog #382800, 1/4" (6mm) Neuro Elastic Retractors, Sterile, Rx only.
Status
Terminated
Initiated
2008-05-12
Posted
2008-09-04
Terminated
2012-04-19
Reason
The bands are breaking within the sealed packaging or in use prior to the expiration dates.
Root cause
Incorrect or no expiration date
Action
Consignees were notified by letter via UPS next day, on/about 05/12/2008. They were instructed to return all affected product or acknowledge that the product no longer exists. They were further instructed to forward the letter to if they have further distributed the affected lots into institutional settings or to homecare patients and retrieve relevant product from those locations. If you require additional information or clarification regarding this matter, please contact Jackie Warner at 1-800-334-9751, ext. 4973.
Quantity
5763 units
Distribution
U.S., Argentina, Australia, Brazil, Canada, Costa Rica, France, Mexico, Puerto Rico, Singapore, and the Virgin Islands
Lot, serial or model codes
Catalog #382800: All manufacturing dates from 4/1/2006 through 3/19/2008; Lot numbers: 01A0800425, 01L0700008, 01L0700339, 01M0700052, 1996009, 2217638, T1206007, T1207101, T1207481, T1209127, T1209524, T1212329, T1212657, T1224116, T1224887, T1226599, T1228526, T1230381, T1232347, T1238489, T1240283, T1242666, T1244664, T1245240,T1238489, T1248506, T1249506, T1253534,T1255173, T1259102, T1278101, T1279049.
510(k) numbers
["K771187"]
PMA numbers
not on file
Product code
GDG
Firm FEI
3005747797
Firm city
Durham
Firm state
NC
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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