Z-0308-05

Easy Go Vac Aspirator, Model PM65HG. Portable suction unit

Name: Z-0308-05 Easy Go Vac Aspirator, Model PM65HG. Portable suction unit
Creator: Precision Medical, Inc.
Published: 2004-11-09
License: https://open.fda.gov/license/

Precision Medical, Inc. / initiated 2004-11-09 / Terminated

FDA source

Precision Medical, Inc. began a recall of Easy Go Vac Aspirator, Model PM65HG. Portable suction unit on 2004-11-09. The reason FDA records is "Battery charger can be overcharged and overheat". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0308-05
Status: Terminated
Initiated: 2004-11-09
Posted: 2004-12-15
Terminated: 2007-06-12
Recalling firm: Precision Medical, Inc.
Product: Easy Go Vac Aspirator, Model PM65HG. Portable suction unit
Product code: BTA Pump, Portable, Aspiration (Manual Or Powered)
Reason for recall: Battery charger can be overcharged and overheat
FDA root cause: Other
Action: The recalling firm sent Recall letters via first class mail on 11/15/04 to their consignees. The recalling firm will replace the chargers free of charge.
Quantity in commerce: 6000 units
Distribution: The product was shipped to medical supply companies and medical facilities nationwide. The product was also shipped to Saudi Arabia, Boliva, Hong Kong, Israel, Brazil, Phillipines, Poland, Canada, Ireland, New Zealand, France, United Kingdom, and Singapore.
Product codes and lots: Serial numbers 008360 through 14360 Charger part number 503974 (Globtek Part # GTM21097CC-5015-1.3 Part No: GS-307-B)

Product code BTA

K971749Class IIEasygo AspiratorPrecision Medical, Inc. / cleared 1998-04-01

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)