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FDA Medical Device Recalls (openFDA)

Becton Dickinson and Company: BD Beaver Arthro-Lok Pointed Tip 4mm Blade, REF 376780. Becton Dickinson and Company, Waltham, MA 02454. Intended for use in arthroscopic procedures.

Recall number
Z-1638-2010
Recalling firm
Becton Dickinson and Company
Product
BD Beaver Arthro-Lok Pointed Tip 4mm Blade, REF 376780. Becton Dickinson and Company, Waltham, MA 02454. Intended for use in arthroscopic procedures.
Status
Terminated
Initiated
2009-06-12
Posted
2010-05-21
Terminated
2012-01-26
Reason
Mislabeled: Arthro-Lok Pointed Tip 4mm Blade curving right instead of left.
Root cause
Packaging process control
Action
Becton Dickinson issued an "Urgent: Field Safety Notice" beginning June 25, 2009 by telephone and letter fax to remove and discard affected product from their possession. Customer verification responses were requested. For further information, contact Becton Dickinson and Company at 1-781-906-7900.
Quantity
354 units
Distribution
Worldwide Distribution -- United States, Japan and Belgium.
Lot, serial or model codes
Lot Number: 7291713, Expiration Date: 2012-10.
510(k) numbers
not on file
PMA numbers
not on file
Product code
HTS
Firm FEI
1211998
Firm city
Waltham
Firm state
MA
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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