CoaguChek brand PT Test Strips; U.S. Catalog Number 3116247 (48 strip pack-professional use), 3116239 (12 strip pack-patient self test), Non-U.S. Catalog Numbers 11937642190 [packaged 48 strips per box] and 11937634190 [packaged 12 strips per box].
FDA Recall Z-0227-2007 · Posted 2006-11-30
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Recalling FirmRoche Diagnostics Corp.
Recall StatusTerminated
Product CodeGJS
Date Initiated2006-10-18
Date Terminated2007-06-20
Product QuantityApprox 26,000,000 test strips to U.S. and 31,000,000 test strips Ex-U.S.
Reason for Recall
Erroneous Test Results: Monitor may display 'error' message or report falsely elevated patient results caused by insufficient amounts of active ingredient (thromboplastin) in the test strips.
Firm Action
A press release was issued by the firm on 10/19/06. The recall letter dated 10/19/06 sent to distributors who sell to home users instructs them to notify their home users and to discard any of product 3116239 in stock. The recall letter dated 10/19/06 to to home users, instructs them to discontinue use of, and to discard, their test strips and to contact their health care professional. The device correction letter dated 10/19/06 to distributors to professional users instructs them to notify customers and provides instructions for duplicate testing in laboratories. The device correction letter dated 10/19/06 to health care professionals asks that they follow-up with their home users to ensure they follow the instructions to cease home use and provides instructions for dupicate testing in laboratories.
Root Cause
Other
Distribution Pattern
Worldwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
K994349COAGUCHEK S SYSTEM, MODEL 2138280Roche Diagnostics Corp. · 2000-09-06K974569COAGUCHEK SYSTEM, COAGUCHEK SYSTEM FOR PROTHROMBIN TIME SELF TESTINGBoehringer Mannheim Corp. · 1998-01-09K962571COAGUCHEK PST SYSTEMBoehringer Mannheim Corp. · 1997-04-22K930454BOEHRINGER MANNHEIM COAGUCHEK SYSTEMBoehringer Mannheim Corp. · 1993-08-05
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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