Zoll Manufacturing LifeVest Wearable Defibrillator Model 4000, Product Number 10A0988-A01 recall — FDA Z-0353-2018
Incorrect service code for properly catching critical defects during self-check. Potential for defibrillation shock failure
Overview of recall records associated with Zoll Manufacturing Corp., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Incorrect service code for properly catching critical defects during self-check. Potential for defibrillation shock failure
This page summarizes recall records in which the official source identifies Zoll Manufacturing Corp. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.