Custom Interventional Pain Management recall: Mastisol Skin Adhesive
Custom Interventional Pain Management, LLC is recalling Mastisol Skin Adhesive – 56. The U.S. Food and Drug Administration published the recall on October 7, 2026; it began on January 15, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Mastisol Skin Adhesive |
| Brand | Custom Interventional Pain Management |
| Company | Custom Interventional Pain Management, LLC |
| Type | Medical devices |
| Classification | Class II |
| Recall date | January 15, 2026 |
| Published by FDA | October 7, 2026 |
| Quantity | 56 |
| Recall ID | 99699 |
Recalled products
- Brand Name: Ferndale Laboratories; Medline; Custom Interventional Pain Management CIPM Product Name: Mastisol Skin Adhesive Model/Catalog Number: 24161B (Ferndale and Medline); Tray 17025 17g continuous PBN tray (CIPM) Software Version: n/a Product Description: Skin Adhesive in a narrow plastic sterilized tube. Mastisol is a skin glue often used during surgical procedures. Continuous epidural trays are designed for use by anesthesiologists and radiologists in the administration of regional anesthesia. Component: surgical kits
- FDA recall number
- Z-0067-2027
- Codes, lots and dates
- 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
- Quantity
- 56
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99699
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- San Antonio, TX, United States
Why it was recalled
The reason the FDA lists: “Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.”
Where it was sold
Nationwide. Distribution as the FDA records it: “U.S. Nationwide distribution in the state of TX.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99699, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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|---|---|---|---|
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| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is Custom Interventional Pain Management Mastisol Skin Adhesive recalled?
Yes. Custom Interventional Pain Management, LLC recalled it on January 15, 2026; FDA published it October 7, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.