Fresh Recalls

Custom Interventional Pain Management recalls

Recall found. Custom Interventional Pain Management is named in FDA Class II recall Z-0067-2027 covering Brand Name. Hazard: Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits. Identifying details: Lot Code: CIPM product / reorder #17025; Description: 17g continuous PBN tray; Item #110026; Received Lot# 27022; Affected Lot #1225271; Expiration Date: 01/31/2028; DHR or Batch Record #64591; UDI: *+B87517LIDO/$$20131281225271T* UDI- DI #: B87517LID0 with Lidocaine. Status: Ongoing.

Models with recalls

Brand Name (1)

All Custom Interventional Pain Management recalls

FDA Class II · Medical device · October 7, 2026

Brand Name recall — Custom Interventional Pain Management, LLC

Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.

Official ID Z-0067-2027 · Official record ↗

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.