Skip to content
Recall Observatory FDA recall evidence

Device product

Dimension TSH Flex Reagent Cartridge (REF RF412). Intended to quantitatively measure human thyroid stimulating hormone (TSH, thyrotropin).

Z-1882-2013

May 10, 2013

Class II

Product summary

Firm
Siemens Healthcare Diagnostics, Inc
Event
Event 65162
Status
Terminated
Classification
Class II
Quantity
39763
Official record key
device-enforcement:Z-1882-2013

Official wording

Reason: A rare variant of TSH, identified in a small cluster of patients, is not detected.

Code information: Per recall strategy.

Distribution pattern: Worldwide Distribution-USA (nationwide) and the countries of Canada, AE, AR, AT, AU, BA, BD, BE, BG, BO, BR, BY, CH, CL, CM, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GR, GT, HK, HN, HR, HU, ID, IE, IL, IN, IR, IS, IT, JO, JP, KA, KR, KW, KZ, LB, LK, LT, LV, LY, MA, MK, MT, MX, MY, NI, NL, NO, NP, OM, PA, PE, PH, PK, PL, PT, PY, QA, RO, RU, SA, SE, SG, SK, SV, SY, TH, TM, TN, TR, TW, UA, UY, UZ, VE, VN, XS, and ZA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    A rare variant of TSH, identified in a small cluster of patients, is not detected.