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Terminated

Precision PCx Test Strips Part Number: 98757-12

FDA Recall Z-0403-03 · Posted 2002-12-31

Recalling FirmAbbott Laboratories, Inc.
Recall StatusTerminated
Product CodeCGA
Date Initiated2002-11-08
Date Terminated2017-02-13
Product Quantity210 packages

Reason for Recall

Use of glucose blood strips may provide false high results

Firm Action

Abbott notified the two hospitals by telephone on 11/8/02. Both responded and returned product.

Root Cause

Other

Distribution Pattern

NC, WI

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K983504PRECISION XTRA ADVANCED DIABETES MANAGEMENT SYSTEM, PRECISION BLOOD GLUCOSE TEST STRIPS, PRECISION XTRA B-KETONE TEST STMedisense, Inc. · 1999-07-09

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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