Vesco Q ENPlus Spike Feed Set recalled for possible dosing inaccuracy
Vesco Medical LLC is recalling Vesco Q ENPlus Spike Feed Sets, model VED-053, because the feeding pump may deliver enteral fluids outside its labeled accuracy of plus or minus 5%. This could cause over- or under-delivery of feeding compared with the prescribed dose. The notice says any effects would likely be temporary or medically reversible, with a remote chance of serious harm, and no injuries have been reported.
From the FDA notice · Read the official notice ↗
What to do
- Contact your care team before changing how you use this feed set.
- Check whether your feed set has UDI-DI 00850002550481 and a lot manufactured through 08/12/2026.
- The notice doesn't say how to get a remedy; contact Vesco Medical LLC.
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- Vesco Q ENPlus Spike Feed Set, Model Numer VED-053
- Sold in
- Nationwide
- Made for
- All ages (under 100 years)
This recall covers 7 products — see all of them.
Details
- Units affected
- 6,060 units
- Illnesses reported
- None reported
- Manufactured in
- 60 Collegeview Rd Space 144, Westerville, Ohio, United States
- Classification
- Class II
- Recall number
- Z-0377-2027
In the FDA's words
- Description
- Vesco Q ENPlus Spike Feed Set, Model Numer VED-053 The feeding pump may deliver enteral fluids outside its labeled accuracy specification of +/-5%. This inaccuracy can result in over-delivery or under-delivery of enteral fluids relative to the prescribed dose, if proper controls are not in place. Over- or under-delivery of enteral nutrition through the pump and associated feed sets could cause temporary or medically reversible adverse health consequences, with a remote probability of serious adverse health consequences. UDI-DI 00850002550481; Lot Numbers: all lots manufactured through 08/12/2026 Distribution: US Nationwide distribution. Affected quantity: 6,060 units
- Hazard
- The feeding pump may deliver enteral fluids outside its labeled accuracy specification of +/-5%. This inaccuracy can result in over-delivery or under-delivery of enteral fluids relative to the prescribed dose, if proper controls are not in place. Over- or under-delivery of enteral nutrition through the pump and associated feed sets could cause temporary or medically reversible adverse health consequences, with a remote probability of serious adverse health consequences.
7 products in this recall
Vesco Q pumps, feed sets recalled for possible dosing inaccuracy
Vesco Medical is recalling 7 Vesco Q products: the Vesco Q Enteral Feeding Pump (model VED-701) and six Vesco Q feed sets (models VED-050, VED-051, VED-052, VED-053, VED-054 and VED-059). The pump may deliver enteral fluids outside its labeled accuracy of plus or minus 5%, so feeds may be over- or under-delivered compared with the prescribed dose. The agency says this could cause temporary or medically reversible effects, with a remote chance of serious harm. No injuries have been reported.
The agency lists each product separately. Check every one you might have.
- Vesco Q Enteral Feeding Pump, Model Number VED-701, Software Versions 6.0 - 7.8Z-0373-2027 · 3,493 units
- Vesco Q 500mL Bag Feed Set (PVC), Model Number VED-050Z-0374-2027 · 121,889 untis
- Vesco Q 1000mL Bag Feed Set (LL), Model Number VED-051Z-0375-2027 · 1,650 units
- Vesco Q 40mm Screw Cap Feed Set, Model Number VED-052Z-0376-2027 · 2,880 units
- Vesco Q ENPlus Spike Feed Set, Model Numer VED-053 (this page)Z-0377-2027 · 6,060 units
- Vesco Q 1000mL Bag Feed Set (PVC), Model Number VED-054Z-0378-2027 · 208,650 units
- Vesco Q 100mL Small Bore Bag Feed Set, Model Number VED-059Z-0379-2027 · 2,220 units