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FDA Medical Device Recalls (openFDA)

Cook Inc.: TFE Coated Curved Newton LLT

Recall number
Z-0963-2018
Recalling firm
Cook Inc.
Product
TFE Coated Curved Newton LLT
Status
Terminated
Initiated
2017-10-13
Posted
not on file
Terminated
2019-10-23
Reason
Label does not state that the product is heparin-coated.
Root cause
Labeling Change Control
Action
On October 31, 2017 an URGENT MEDICAL DEVICE CORRECTION was issued to customers requesting the following, including a corrective action: Step 1: Determine if your product is included in the affected lot ranges by comparing your lot number to the listing provided. " If your product is not affected, complete the Acknowledgement and Receipt Form. " If your product is affected, proceed to Step 2. Step 2: Remove a Heparin Coated label from the label sheet provided and apply to the top right corner of your affected unit. o If you need additional labels, please contact Stericycle at 855.215.4967. If you would like assistance, representatives are available to support you. To request assistance, please contact Stericycle at 855.215.4967
Quantity
3,364
Distribution
Nationally
Lot, serial or model codes
Catalog # TSCFNB-35-180-SPENCERMOD- BH Affected lots to include: 3741882 - 6142463 F3884311 - F4903643 NS5044201 - NS5963180
510(k) numbers
not on file
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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