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FDA Medical Device Recalls (openFDA)

Terumo Medical Corporation: Pinnacle Destination Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.

Recall number
Z-1611-2013
Recalling firm
Terumo Medical Corporation
Product
Pinnacle Destination Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.
Status
Terminated
Initiated
2013-05-30
Posted
2013-06-27
Terminated
2013-10-30
Reason
Medical devices were incorrectly labeled with extended expiration dates.
Root cause
Error in labeling
Action
The recalling firm notified consignees by letter on 5/30/2013. The letter was flagged as an urgent product bulletin addressed to risk managers. The notification advised customers to immediately discontinue use and quarantine any available stock for subsequent instructions to be provided for pick-up and replacement.
Quantity
20 units
Distribution
Nationwide Distribution.
Lot, serial or model codes
Lot MM27
510(k) numbers
["K091329"]
PMA numbers
not on file
Product code
DYB
Firm FEI
1118880
Firm city
Elkton
Firm state
MD
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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