FDA recall record

Polymer Technology Systems Lipid Panel test strips, REF 1710, also private labeled under recall — FDA Z-1371-2019

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…

Class IIclassification
Z-1371-2019official record ID
May 29, 2019report date

Recall record at a glance

Official recordZ-1371-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPolymer Technology Systems, Inc.
Report dateMay 29, 2019
Recall initiation dateJan 16, 2019
Quantity67643 total
LocationIndianapolis, IN, United States

Official product description

Lipid Panel test strips, REF 1710, also private labeled under Henry Schein as REF 570-0414

Why the product was recalled

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.

Distribution information

Domestic distribution nationwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.