FDA recall record

Maquet SAS VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June recall — FDA Z-1937-2018

Potential keypad failure on VOLISTA StandOP Surgical Lights.

Class IIclassification
Z-1937-2018official record ID
Jun 6, 2018report date

Recall record at a glance

Official recordZ-1937-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMaquet SAS
Report dateJun 6, 2018
Recall initiation dateApr 19, 2018
Quantity187
LocationOrleans, N/A, France

Official product description

VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref. ARD568801560; Part numbers: 568811901, VLT600SF AIM STP; 568811911, VLT600SF AIM STP; 568811961, VLT600DF AIM STP; 568821910, VLT600SF STP QL; 568821911, VLT600SF AIM STP QL; 568821960, VLT600DF STP QL; 568821961, VLT600DF AIM STP QL VOLISTA surgical lights are intended to be used to provide visible illumination of the surgical area or patient during surgical operations, diagnostics and treatment.

Why the product was recalled

Potential keypad failure on VOLISTA StandOP Surgical Lights.

Distribution information

Worldwide Distribution: US (nationwide) and countries of: (AE, AR, AT, AU, BD, BE, BO, BR, CA, CH, CL, CM, CN, CO, CZ, DE, DK, EC, EE, EG, ES, Fl, FR, GB, GH, HK, HR, HU, IE, IN, IQ, IR, IT, JO, JP, KE, KR, LB, LU, LV, MQ, MX, MY, NA, NG, NL, OM, PA, PK, PL, PT, PY, RO, RS, SA, SE, SG, SI, SK, TH, TR, TT, TW, TZ, YE, ZA, ZW).

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

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