CLASS I ONGOING Device recall · Reported 18 Jun 2025 · FDA Enforcement Report

Z-800W Infusion System recalled by Zyno Medical

Zyno Medical is recalling Z-800W Infusion System, distributed nationwide in the US. The recall was initiated on 7 May 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesModel Number: Z800W; UDI-DI; 00814371020020; Serial No. 700063; 700163; 700203; 700402; 700488; 700093; 700169; 700210; 700428; 700495; 700104; 700172; 700214; 700431; 700503; 700111; 700188; 700225; 700440; 700510; 700120; 700189; 700230; 700449; 700513; 700135; 700190; 700285; 700460; 700541; 700145; 700192; 700375; 700471; 700481; 700150; 700195; 700391; 700472; 700397; 700159; 700199; 700393; 700478; 700201; 700162.
Quantity recalled613 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1867-2025
FDA event ID
96796
Recalling firm
Zyno Medical, Natick, MA
Classification
Class I
Status
Ongoing
Recall initiated
7 May 2025
FDA classified
6 Jun 2025
Reported
18 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Device Malfunction

Timeline

7 May 2025Recall initiated by company
6 Jun 2025Classified by FDA+30 days
18 Jun 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Unreleased software versions were installed on distributed devices without verification or validation.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Z-800W Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.

Where it was distributed

US Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Unreleased software versions were installed on distributed devices without verification or validation.

Which lots are affected?

Model Number: Z800W; UDI-DI; 00814371020020; Serial No. 700063; 700163; 700203; 700402; 700488; 700093; 700169; 700210; 700428; 700495; 700104; 700172; 700214; 700431; 700503; 700111; 700188; 700225; 700440; 700510; 700120; 700189; 700230; 700449; 700513; 700135; 700190; 700285; 700460; 700541; 700145; 700192; 700375; 700471; 700481; 700150; 700195; 700391; 700472; 700397; 700159; 700199; 700393; 700478; 700201; 700162.

Where was it sold?

US Nationwide

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 96796

This product is part of a recall event; the main page for the event is Z-800 Infusion System recalled by Zyno Medical.

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