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Abbott Point of Care, i-STAT CREA Cartridge (Creatine/Crea) recallZ-0373-2008 · Abbott Point of Care Inc. · initiated Oct 18, 2007

Terminated All recalls posted in December 2007

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 Abbott Point of Care Inc. 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

Difficult to Close -- Certain lots of i-STAT cartridges are difficult to close, will not close or do not stay closed.

FDA root cause category: Packaging change control

What the company is doing

Abbott Point of Care sent and Urgent Notice to all i-STAT Customers (US and Canadian consignees) notifying them that certain lots of i-STAT cartridges have snap closures that are difficult to close, will not close or do not stay closed. The customers were asked to review the lot numbers on the enclosure and, if the facility has any cartridges from the lot numbers listed, they should remove from service immediately.

Recall details

Recall number
Z-0373-2008
Recall class
Not yet classified by the FDA
Status
Terminated
Initiated by the company
Oct 18, 2007
Posted by the FDA
Dec 11, 2007
Recalling firm
Abbott Point of Care Inc.
Product code
JGS
FDA submissions
K973292
Distribution
Worldwide Distribution- including USA and country of Canada.

Product description

Abbott Point of Care, i-STAT CREA Cartridge (Creatine/Crea); List No: 06F10-01; Part No: 320100; Abbott Point of Care Inc., East Windsor, NJ 08520 USA; Product of Canada.

Code information (models, lots, serial numbers)

Catalog Number: 06F10-01; 06F10-02 Lot Numbers: A07149; A07150; G07121; G07148; G07150; G07151; G07151A; G07157; G07158; and G07164A.

Other devices under the same FDA submission

1 device cleared under K973292 — 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 44972).

Sources and updates

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