Z-1736-2010

EVA 450 Patient Lift Battery Charger

Name: Z-1736-2010 EVA 450 Patient Lift Battery Charger
Creator: Romedic, Inc.
Published: 2010-04-28
License: https://open.fda.gov/license/

Romedic, Inc. / initiated 2010-04-28 / Terminated

FDA source

Romedic, Inc. began a recall of EVA 450 Patient Lift Battery Charger on 2010-04-28. The reason FDA records is "Incorrect battery chargers were supplied with the EVA 450 Patient Lifts. Charger unit stops working and will not charge lift. New chargers were supplied to customers". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1736-2010
Status: Terminated
Initiated: 2010-04-28
Posted: 2010-06-01
Terminated: 2010-09-30
Recalling firm: Romedic, Inc.
Product: EVA 450 Patient Lift Battery Charger.
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: Incorrect battery chargers were supplied with the EVA 450 Patient Lifts. Charger unit stops working and will not charge lift. New chargers were supplied to customers.
FDA root cause: Other
Action: The recalling firm sent out a letter with instructions as follows: 1) Locate EVA 450 Patient Lift(s), 2) Fill out Customer Response Form and fax to 888-691-1091, 3) Replace battery charger(s) with new battery charger(s) supplied with this notification; NEW battery charger to be used according to EVA 450 Instructions, 4) Repackage replaced battery charger(s) in original packing in which shipment was recieved, 5) Apply supplied sticker "EVA 450 Battery Charger RECALL" on outside of box, 6) Apply supplied UPS return label on outside of box and contact UPS for pickup and mail to the following Address: RoMedic, Inc., 300 West Chestnut St., Ephrata, PA 17522; Attn: EVA 450 Battery Charger Recall. Additional questions are directed to the company at phone: 888-625-4343.
Quantity in commerce: 76 units
Distribution: Nationwide distribution.
Product codes and lots: Serial numbers: 373317696102209, 373317696102210, 373317696102224, 373317696102227, 373317696102228, 373317696102232, 373317696102235, 373317696102242, and 373317696102244.

Product code FSA

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)