Data Foundry

Medical device recalls 2023

Sterile surgical convenience kits: 1 — Class II medical device recall Z-1437-2023

Ongoing recall by ROi CPS LLC, reported 2023-05-03, distributed nationwide. The recalling firm was notified by their supplier that the light handle covers may separate from the light han

Recall numberZ-1437-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmROi CPS LLC, Republic, MO, United States
Recall initiated2023-03-22
Classified2023-04-25
Reported by FDA2023-05-03
DistributedNationwide (US)
Quantity456 kits
UPC / GTIN / UDI-DI10194717110880, 10194717111023, 10194717112242, 10194717112709, 10194717114130
Lot numbers95309, 95370, 95477, 95506, 95632, 95646
Model numbers800716005, 800756005, 880387005, 880396007, 880411008, NU00921E, NU00961EOH, NU00991E, NU01001G, NU01018H
Expiration dates2024-05-30, 2024-05-31, 2024-06-30, 2024-10-29, 2024-11-15

Product

Sterile surgical convenience kits: 1. regard Item Number: 800756005, NU00961E - OH Laminectomy Cust Pack; 2. regard Item Number: 880411008, NU01018H - Lumbar Universal ; 3. regard Item Number: 880396007, NU01001G - Craniotomy ; 4. regard Item: 880387005, NU00991E - Ant/Cervical Spine ; and 5. regard Item Number: 800716005, NU00921E - ORMC Major Crani Pack.

Reason for recall

The recalling firm was notified by their supplier that the light handle covers may separate from the light handle and fall off during use. The light handle covers are a kit component.

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-1437-2023. 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.