Data Foundry

Medical device recalls 2014

Tonometers are manual devices intended to measure intraocular… — Class II medical device recall Z-0558-2015

Terminated recall by Instrumed International, Inc., reported 2014-12-17, distributed nationwide. The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market the

Recall numberZ-0558-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmInstrumed International, Inc., Schaumburg, IL, United States
Recall initiated2014-09-08
Classified2014-12-08
Reported by FDA2014-12-17
Terminated2017-11-29
DistributedNationwide (US)
Quantity23 tonometers
Lot numbers030212, 030413, 040113, 100312, 120113
Model numbers3-5754, 60-6031, 80-9010, AM0530, MDG0781649

Product

Tonometers are manual devices intended to measure intraocular pressure by applying a known force on the globe of the eye and measuring the amount of indentation produced (Schiotz type) or to measure intraocular tension by applanation (applying a small flat disk to the cornea) and are sold under the Millennium Surgical, Symmetry Surgical, Accutome, Boss Instruments, and Medline Industries brand names.

Reason for recall

The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as "Pre-Amendment" devices.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0558-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.