Lipid Panel test strips, REF 1710, also private labeled under Henry Schein as REF 570-0414
FDA Recall Z-1371-2019 · Posted None
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Recalling FirmPolymer Technology Systems, Inc.
Recall StatusTerminated
Product CodeCHH
Date Initiated2019-01-16
Date Terminated2020-06-24
Product Quantity67643 total
Reason for Recall
Some lots of test strips do not fit tightly into the optical block, and may fall out during analysis, which could lead to an incorrect result being displayed.
Firm Action
The firm initially notified some of their customers from January through March 2019 with a Customer Bulletin. On March 28, 2019, the firm issued an updated Urgent Medical Device Recall letter to all affected customers. The letter alerted customers to the potential for test strips to slip out of the analyzer.
Actions to be taken by the Customer/User:
1. Closely follow the instructions for proper testing.
" Make sure the analyzer is sitting on a flat, stable surface. Do not perform testing with the analyzer held in the hand.
" After inserting the test strip(s), do not move the analyzer until testing is complete and the test strip is removed.
" As stated in the instructions for use, if an unexpected test result is given, the test should be repeated.
There is no need to return or destroy the product.
2. Distributors should immediately forward this notice to all customers/users who may have received this product.
3. Acknowledge receipt of this instruction by completing the attached form, even if you do not have affected product on hand.
If you have any questions, please contact Karmen Mercer, Director of Global Customer Care directly, Monday through Friday, 8:00 AM to 5:00 PM, Eastern Time at +1 317-870-5610 or (U.S. toll-free) 877-570-8610.
Root Cause
Device Design
Distribution Pattern
Domestic distribution nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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