Recall Z-1810-2025— MEDLINE INDUSTRIES, LP - Northfield

Name: FDA recall Z-1810-2025
Creator: U.S. Food and Drug Administration
Published: 2025-04-22

Class I · Ongoing

Class I FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2025-04-22. It names one FDA 510(k) clearance: K213481. Product: Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C. Reason: Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate..

Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Classification: Class I
Status: Ongoing
Initiated: 2025-04-22
Firm location: Northfield, IL, United States

510(k) clearances named in this recall

1 on FDA's record

K213481 — Medline General Surgery TrayMedline Industries, Inc.·cleared 2022-05-24

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C

Reason for recall

Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.

Data sourced from openFDA. This site is unofficial and independent of the FDA.