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FDA Medical Device Recalls (openFDA)

Cook, Inc.: THSCF-35-260-3-AUS2, (Cook Vascular Wire Guide, PTFE coated curved Amplatz ultra stiff catheter exchange, Diameter .035 Inch, length 260 cm, curve radius 3 mm, Cook Incorporated, Bloomington, IN 47402 - not on label)

Recall number
Z-0135-2008
Recalling firm
Cook, Inc.
Product
THSCF-35-260-3-AUS2, (Cook Vascular Wire Guide, PTFE coated curved Amplatz ultra stiff catheter exchange, Diameter .035 Inch, length 260 cm, curve radius 3 mm, Cook Incorporated, Bloomington, IN 47402 - not on label)
Status
Terminated
Initiated
2007-08-15
Posted
2008-02-06
Terminated
2008-04-21
Reason
The device is normally sold as sterile, however this lot was not sterilized and the device is not adequately labeled, as the label does not state whether the device is sterile or non-sterile and lacks the manufacturer's name and address.
Root cause
Process control
Action
Cook Incorporated notified consignees by Urgent Product Recall letter dated 8/15/07 instructing them to return the product.
Quantity
33
Distribution
Worldwide Distribution - USA, Australia, India, Trinidad and Tobago.
Lot, serial or model codes
Lot E2026214.
510(k) numbers
["K832178"]
PMA numbers
not on file
Product code
DQX
Firm FEI
1820334
Firm city
Bloomington
Firm state
IN
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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