Data Foundry

Medical device recalls 2017

Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 — Class II medical device recall Z-1777-2017

Terminated recall by Welch Allyn Inc, reported 2017-04-19, distributed nationwide. A defective electrical component in the battery charging circuit in two lots of the ProBP 2400 may potentially

Recall numberZ-1777-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmWelch Allyn Inc, Skaneateles Falls, NY, United States
Recall initiated2017-02-27
Classified2017-04-11
Reported by FDA2017-04-19
Terminated2019-06-14
DistributedNationwide (US)
Quantity981 units
Lot numbers0715, 1215
Model numbers901096

Product

Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch Allyn Inc., 4341 State Street Road, Skaneateles Falls, NY 13153 --- Microlife Corporation 9F, 431, RuiGuang Road, NeiHu, Taipei, 11492, Taiwan, R.O.C. --- Microlife AG Espenstrasse 139 9443 Widnau, Switzerland

Reason for recall

A defective electrical component in the battery charging circuit in two lots of the ProBP 2400 may potentially cause an over-voltage battery charging condition when the device is connected to the external power supply/battery charger. This potential defect resides with the device, not the battery. The over-voltage condition can result in high NiMH battery temperatures that, in some cases, can reach levels sufficient to cause melting of the plastic battery door and other adjacent plastic and foam device components.

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-1777-2017. 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.