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Interlink System Continu-Flo Solution Set with Microbore… recallZ-1152-03 · Baxter Healthcare Corp. · initiated Jul 16, 2003

Terminated All recalls posted in August 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 Baxter Healthcare Corp. 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

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDA root cause category: Other

What the company is doing

Recalled by letter dated 7/16/03. The accounts were informed of the potential for leaks in the set tubing, and asked to inspect their inventory for the affected product codes and lots, segregate any affected products found and discard them according to local procedures. The customers will receive credit for the discarded affected product.

Recall details

Recall number
Z-1152-03
Recall class
Not yet classified by the FDA
Status
Terminated
Initiated by the company
Jul 16, 2003
Posted by the FDA
Aug 21, 2003
Recalling firm
Baxter Healthcare Corp.
Quantity
3,456 units
Product code
FPA
FDA submissions
K961225
Distribution
Nationwide, Mexico, Canada, Columbia, Australia, New Zealand and Taiwan

Product description

Interlink System Continu-Flo Solution Set with Microbore Tubing, 60 drops/mL, 128'', 3 injection sites, Male Luer Lock Adapter, catalog 2C6521; Baxter Healthcare Corporation, Deerfield, IL 60015 USA

Code information (models, lots, serial numbers)

catalog 2C6521, lot numbers UR117432 through UR167015. Please note: Baxter lot numbers are represented by an internal reference code ''UR'' followed by a six digit sequential number, or by the letter ''U'' followed by a six digit sequential number with and ''R'' suffix. Any lot number appearing within the identified six digit sequential number range is subject to the recall.

Other devices under the same FDA submission

24 devices cleared under K961225 — 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 26772).

Sources and updates

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