FDA Medical Device Recalls (openFDA)
Codman & Shurtleff, Inc.: Codman Disposable Twist Drill Product code: 80-1200 This is a single use, disposable drill kit designed for gaining access to the cranium for therapeutic and/or diagnostic procedures
- Recall number
- Z-2028-2011
- Recalling firm
- Codman & Shurtleff, Inc.
- Product
- Codman Disposable Twist Drill Product code: 80-1200 This is a single use, disposable drill kit designed for gaining access to the cranium for therapeutic and/or diagnostic procedures
- Status
- Terminated
- Initiated
- 2010-11-30
- Posted
- 2011-04-20
- Terminated
- 2013-03-14
- Reason
- Packaging defect may compromise sterility of device
- Root cause
- Package design/selection
- Action
- The firm, Codman, sent an "Important Notice Urgent- Voluntary Product Recall Notification" letter dated November 30, 2010 to its customers via FedX. On January 7, 2011, Codman expanded the recall to four additional product codes.On January 31, 2011, the firm issued a supplemental recall letter and identified one additional product code: 80-11197. The letters described the product, problem and actions to be taken. The customers were instructed to identify the unused affected products in their inventory and follow the recall instructions provided: 1) If you have NO product to return, please advise Codman as soon as possible using the FACSIMILE form attached and fax to 508-828-6118 and 2) if you DO have product to return, please call 1-800-225-0460, Option 4, for instructions for return. Codman is presently working toward supplying replacement products as soon as possible. Please call Customer Service to check on the status of product availability at 1-800-225-0460. Should you have any questions regarding this recall, please call Customer Service at 1-800-225-0460 or your local Codman Representative.
- Quantity
- 1549 units
- Distribution
- Worldwide distribution: USA including states of :AL, FL,GA, KY, MA, MI, MN, MS, OR, PA, RI, UT,WI and WV; and countries including: Argentina, Australia, Canada, Bahamas , Belgium, Dubai, Japan, Madrid, Mexico, New Zealand, Saudia Arabia, UAE, Uruguay, and United Kingdom.
- Lot, serial or model codes
- Lot Codes: JA292; KA243; LA259; AB273; LB308; AC267; CB286; EB229; EB356 ; EB327; JB306; LB308; 422004; 422005; 422006; 429017; 430536
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GWM
- Firm FEI
- 3002947440
- Firm city
- Raynham
- 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
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
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