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FDA Medical Device Recalls (openFDA)

Haemonetics Corporation: Haemonetics High Speed Cell Saver Bowl Set List Number: 263

Recall number
Z-0501-03
Recalling firm
Haemonetics Corporation
Product
Haemonetics High Speed Cell Saver Bowl Set List Number: 263
Status
Terminated
Initiated
2002-12-17
Posted
2003-01-30
Terminated
2016-01-28
Reason
Disposable Set for Autologous Blood recovery may leak saline at the Y-connector
Root cause
Other
Action
Haemonetics notified accounts of the recall on December 17, 2002 by fax. A hard copy of the same letter was sent to each customer via certified mail, return receipt on December 18 and 19. Users are requested to cease use of product and return product to Haemonetics.
Quantity
11302
Distribution
Nationwide Canada
Lot, serial or model codes
J02115 J02131 J02142 J02150 J02162 G02081 G02086 G02092 G02103 G02133 G02141 H02007 H02015 H02024 H02038 H02102 H02108 H02120 H02147 H02157 H02165 H02239 H02249 J02032 J02040 J02049 J02058 J02061 J02076 J02172 J02194 J02208 K02015 K02027 K02037 K02045 K02056 K02066 K02139 K02161 K02171 K02208 K02217 K02224 K02236 L02002 L02049 L02059 L02093 L02103 L02113 L02144 L02163 L02199 M02002 M02010 M02014 M02022 M02027 M02035
510(k) numbers
["K932890"]
PMA numbers
not on file
Product code
CAC
Firm FEI
1219343
Firm city
Braintree
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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