Custom Interventional Pain Management recalls

Custom Interventional Pain Management has 1 recall on record with the FDA and USDA, the earliest in 2026 and the latest reported on 7 Oct 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is foreign material.

Total recalls1since 2026

Last 12 months1reported

Class I00% of total

Ongoing1latest 7 Oct 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 1

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why custom interventional pain management is recalled

Foreign Material1100%

Product types

Surgical Instruments1100%

By year

20261100%

Ongoing custom interventional pain management recalls

1 active

Reported	Class	Recall	Company	Reason	Where
7 Oct 2026Device	CLASS II	Ferndale Laboratories recalled by Custom Interventional Pain	Custom Interventional Pain Management	Foreign Material	Nationwide

All custom interventional pain management recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
7 Oct 2026Device	CLASS II	Ferndale Laboratories recalled by Custom Interventional Pain	Custom Interventional Pain Management	Foreign Material	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.