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FDA Medical Device Recalls (openFDA)

Remel Inc: PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.

Recall number
Z-2350-2015
Recalling firm
Remel Inc
Product
PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of beta-hemolytic streptococci of Lancefield Groups A, B, C, F or G from primary culture plates.
Status
Terminated
Initiated
2015-06-30
Posted
2015-08-07
Terminated
2017-02-13
Reason
A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.
Root cause
Under Investigation by firm
Action
On 4/28/2015, the recalling firm's European subsidiary notified the recalling firm of the recall. On 6/30/2015, the recalling firm notified their customers of the recall via letter, sent USPS standard mail.
Quantity
1859 kits
Distribution
Nationwide Distribution, including Puerto Rico and the country of Canada.
Lot, serial or model codes
lot 1470133, exp. date 31 Mar 2016
510(k) numbers
not on file
PMA numbers
not on file
Product code
GTY
Firm FEI
1924669
Firm city
Lenexa
Firm state
KS
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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