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Haemonetics Cell Saver 5 Low Volume (125mL) Fast Pack recallZ-0502-03 · Haemonetics Corporation · initiated Dec 17, 2002

Terminated All recalls posted in January 2003

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Haemonetics Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Disposable Set for Autologous Blood recovery may leak saline at the Y-connector

FDA root cause category: Other

What the company is doing

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.

Recall details

Recall number
Z-0502-03
Recall class
Not yet classified by the FDA
Status
Terminated
Initiated by the company
Dec 17, 2002
Posted by the FDA
Jan 30, 2003
Recalling firm
Haemonetics Corporation
Quantity
2430
Product code
CAC
FDA submissions
K932890
Distribution
Nationwide Canada

Product description

Haemonetics Cell Saver 5 Low Volume (125mL) Fast Pack List Number: 265

Code information (models, lots, serial numbers)

KK02003 KK02011 KK02012 KK02014 KK02020 KK02100 LL02001 LL02009 LL02015 LL02022

Other devices under the same FDA submission

2 devices cleared under K932890 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 25342).

Sources and updates

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