Data Foundry

Medical device recalls 2023

Sprint 200 wheeled stretcher — Class II medical device recall Z-1211-2023

Ongoing recall by Linet Spol. S.r.o., reported 2023-03-15, distributed in AL, CA, FL, IA, KY, LA, MN, NC…. Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patie

Recall numberZ-1211-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmLinet Spol. S.r.o., Zelevcice, Czech Republic
Recall initiated2023-01-18
Classified2023-03-03
Reported by FDA2023-03-15
DistributedAL, CA, FL, IA, KY, LA, MN, NC, NV, OK, TX, VA, WA, WV
Countries outside the USAU, BE, BH, CA, CH, DE, GB, IT, SG, ZA
Reason classeslabeling
UPC / GTIN / UDI-DI08592654356678, 08592654356685, 08592654358467
Serial numbers20220190528, 20220190530, 20220190537, 20220190539, 20220190540, 20220190543, 20220190544, 20220190548, 20220190550, 20220190552, 20220190554, 20220203402, 20220203404, 20220203407, 20220203420, 20220203422, 20220203425, 20220203427, 20220203428, 20220203429, 20220203430, 20220203836, 20220203841, 20220203850, 20220203852 and 125 more
Model numbers1ES200-7, 1ES210-1, 1ES211-1

Product

Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.

Reason for recall

Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.

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-1211-2023. 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.