Z-800F Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and...
FDA Device Recall #Z-1866-2025 — Class I — May 7, 2025
Recall Summary
| Recall Number | Z-1866-2025 |
| Classification | Class I — Serious risk |
| Date Initiated | May 7, 2025 |
| Status | Ongoing |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Zyno Medical LLC |
| Location | Natick, MA |
| Product Type | Devices |
| Quantity | 613 units |
Product Description
Z-800F Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Reason for Recall
Unreleased software versions were installed on distributed devices without verification or validation.
Distribution Pattern
US Nationwide
Lot / Code Information
Model No: Z800F; UDI-DI: 00814371020013; Serial No. 600091; 600133; 600203; 600259; 600320; 600361; 600404; 600446; 600482; 600526; 600565; 600601; 600094; 600138; 600204; 600261; 600321; 600362; 600406; 600447; 600483; 600528; 600566; 600603; 600095; 600139; 600206; 600262; 600322; 600363; 600407; 600449; 600485; 600529; 600568; 600604; 600099; 600141; 600207; 600263; 600323; 600364; 600408; 600450; 600487; 600531; 600569; 600605; 600100; 600142; 600209; 600265; 600324; 600369; 600410; 600451; 600488; 600532; 600570; 600608; 600102; 600143; 600211; 600266; 600325; 600370; 600411; 600452; 600489; 600533; 600571; 600609; 600104; 600146; 600215; 600267; 600326; 600376; 600412; 600453; 600490; 600535; 600572; 600610; 600105; 600148; 600217; 600268; 600328; 600377; 600414; 600454; 600495 600536; 600573; 600611; 600106; 600150; 600220; 600270; 600330; 600378; 600415; 600456; 600496; 600539; 600574; 600612; 600108; 600151; 600223; 600271; 600331; 600379; 600416; 600457; 600498; 600540; 600575; 600613; 600109; 600152; 600224; 600289; 600335; 600383; 600417; 600458; 600499; 600541; 600576; 600614; 600110; 600153; 600227; 600292; 600336; 600384; 600418; 600460; 600504; 600542; 600577; 600615; 600111; 600154; 600228; 600294; 600338; 600385; 600419; 600461; 600505; 600543; 600578; 600617; 600112; 600155; 600229; 600295; 600339; 600386; 600422; 600462; 600506; 600545; 600579; 600618; 600113; 600156; 600230; 600297; 600341; 600387; 600423; 600464; 600509; 600546; 600580; 600921; 600114; 600157; 600231; 600298; 600342; 600388; 600424; 600465; 600510; 600549; 600583; 601325; 600115; 600158; 600235; 600299; 600343; 600389; 600425; 600466; 600511; 600551; 600584; 601433; 600116; 600159; 600238; 600300; 600344; 600391; 600427; 600467; 600513; 600553; 600585; 601514; 600118; 600160; 600239; 600301; 600347; 600392; 600430; 600470; 600514; 600554; 600586; 601603; 600120; 600161; 600240; 600302; 600348; 600393; 600431; 600471; 600516; 600555; 600587; 601651; 600121; 600162; 600249; 600303; 600349; 600394; 600432; 600473; 600517; 600556; 600589; 602578; 600122; 600164; 600250; 600304; 600350; 600396; 600436; 600474; 600518; 600557; 600591; 602743; 600126; 600165; 600251; 600305; 600351; 600398; 600437; 600475; 600519; 600558; 600592; 602807; 600127; 600168; 600252; 600306; 600352; 600399; 600438; 600476; 600520; 600559; 600594; 603858; 600129; 600174; 600253; 600308; 600353; 600400; 600440; 600477; 600521; 600560; 600595; 604637; 600130; 600176; 600254; 600309; 600356; 600401; 600442; 600478; 600522; 600562; 600596; 605411; 600131; 600188; 600255; 600310; 600357; 600402; 600443; 600480; 600523; 600563; 600599; 605870; 600132; 600192; 600257; 600319; 600359; 600403; 600445; 600481; 600525; 600564; 600600; 605918; 605964; 606886; 607077; 607891; 608058; 608061; 608612; 613123; 614776.
Other Recalls from Zyno Medical LLC
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-1865-2025 | Class I | Z-800 Infusion System. Intended to provide intr... | May 7, 2025 |
| Z-1868-2025 | Class I | Z-800WF Infusion System. Intended to provide in... | May 7, 2025 |
| Z-1867-2025 | Class I | Z-800W Infusion System. Intended to provide int... | May 7, 2025 |
| Z-0506-2025 | Class II | Z-800 Infusion System. Model/Catalog Number: Z-... | Oct 18, 2024 |
| Z-0523-2025 | Class III | Brand Name: Z-800 Infusion System Product Name... | Sep 30, 2024 |
Frequently Asked Questions
A software recall means the device's embedded software or firmware has a defect that could affect its performance or safety. Many software recalls are corrected through firmware updates that can be applied without physically replacing the device. For implantable devices, the update may be delivered wirelessly during a routine clinic visit. For external devices, the manufacturer may provide updated software files or replacement units. Contact your healthcare provider to determine whether your specific device and software version are affected and what action is recommended.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.