Data Foundry

Medical device recalls 2020

Type S Extension For use with Varian — Class II medical device recall Z-2243-2020

Terminated recall by Med Tec Inc, reported 2020-06-10, distributed nationwide. Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associ

Recall numberZ-2243-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMed Tec Inc, Orange City, IA, United States
Recall initiated2020-05-12
Classified2020-06-02
Reported by FDA2020-06-10
Terminated2021-03-25
DistributedNationwide (US)
Countries outside the USCO, CR, ES, HU, IT, KR, SA
Quantity171 units
UPC / GTIN / UDI-DI00841439104156
Lot numbersM027990, M166160, M198170, M241650, M249180, M257630, M278760, M282330, M283380, M293670, M300750, M303010, M314410, M321880, M323560, M326580, M333420, M350700, M356130, M362290, M365740, M369700, M371990, M418080, M436620, M439700, M442410, M446460, M448260, M457870, M457880, M462640, M493710, M495030, M505880, M505890, M505900, M505910, M511240, M530920 and 48 more

Product

Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning.

Reason for recall

Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2243-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.