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FDA Medical Device Recalls (openFDA)

Becton Dickinson & Co.: BBL (TM) LIM Broth, in glass slant tubes and packaged 100 tubes per carton, catalog #296266.

Recall number
Z-1294-03
Recalling firm
Becton Dickinson & Co.
Product
BBL (TM) LIM Broth, in glass slant tubes and packaged 100 tubes per carton, catalog #296266.
Status
Terminated
Initiated
2003-08-11
Posted
2003-10-15
Terminated
2003-11-19
Reason
Broth for growing selective bacteria may fail to inhibit overgrowth of gram negative microorganisms resulting in the inability to isolate Group B Streptococci.
Root cause
Other
Action
Recalling firm notified distributors and end user by letter 8/11/03 and advised of product failure. Consignees were requested to discontinue distribution and use and discard product for replacment. Consignees were requested to return response form.
Quantity
860 cartons
Distribution
Product was sold to 11 distributors and one end user in the US. Product was additionally distributed to firm''s subsidiaries in Canada and Europe.
Lot, serial or model codes
Lot numbers: 3129508 exp 1/30/04 3129509 exp 2/3/04 3129506 exp 2/3/04 3129512 exp 2/3/04
510(k) numbers
not on file
PMA numbers
not on file
Product code
JSD
Firm FEI
1119779
Firm city
Sparks
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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