Pro-Med Instruments recalls

Pro-Med Instruments has 5 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 4 Jun 2025. 1 is still ongoing. The most frequent reason is lead & heavy metals.

Total recalls5since 2017

Last 12 months0reported

Class I360% of total

Ongoing1latest 4 Jun 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 1 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 3 60%Class II 2 40%Class III 0 0%

Why pro-med instruments is recalled

Product types

Spinal Implants360%
Other Medical Devices240%

By year

2025120%
2018360%
2017120%

Ongoing pro-med instruments recalls

1 active

Reported	Class	Recall	Company	Reason	Where
4 Jun 2025Device	CLASS II	DORO¿ Easy-Connect Navigation Adaptor recalled by Pro-Med Instruments	Pro-Med Instruments	Other	Nationwide

All pro-med instruments recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
4 Jun 2025Device	CLASS II	DORO¿ Easy-Connect Navigation Adaptor recalled by Pro-Med Instruments	Pro-Med Instruments	Other	Nationwide
26 Sep 2018Device	CLASS I	Doro Lucent Locking Transitional Member recalled by Pro-Med Instruments	Pro-Med Instruments	Lead & Heavy Metals	7 states
26 Sep 2018Device	CLASS I	Doro Lucent Base Unit recalled by Pro-Med Instruments	Pro-Med Instruments	Lead & Heavy Metals	7 states
26 Sep 2018Device	CLASS I	Doro Lucent Transitional Member recalled by Pro-Med Instruments	Pro-Med Instruments	Lead & Heavy Metals	7 states
13 Dec 2017Device	CLASS II	pmi, pro med instruments, DORO(R) Sterile Disposable Skull recalled	Pro-Med Instruments	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.