Data Foundry

Medical device recalls 2024

natus neurology — Class II medical device recall Z-1306-2024

Ongoing recall by Natus Neurology Inc, reported 2024-03-27, distributed nationwide. Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall

Recall numberZ-1306-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmNatus Neurology Inc, Middleton, WI, United States
Recall initiated2024-02-07
Classified2024-03-19
Reported by FDA2024-03-27
DistributedNationwide (US)
Countries outside the USCA
Quantity35 units
Lot numbers122923, 614921, 614922, 614923, 628166
Model numbers024252

Product

natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252

Reason for recall

Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Number A0623009. They have received five complaints. These customers reported that the gel is too thick, is discolored (darker than usual), and in one instance, patients reported irritation after procedures using the gel.

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-1306-2024. 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.