Lower risk Medical device recall · FDA · Published September 26, 2025

Integra NeuroSciences Recalls CODMAN Disposable Perforators for Inadequate Welds

Integra NeuroSciences recalls CODMAN Disposable Perforators 11mm and 9mm models with inadequate welds. Affected units have specific lot numbers and expiration dates. Consumers should check their product details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0373-2026Medical device Integra NeuroSciences ›

Lower-risk recall

Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.

Take action

Contact the company

Recalling firmIntegra LifeSciences Corp. (NeuroSciences)1100 Campus Rd · Princeton, NJ 08540-6650

✎ GovInfoNow plain-language explainer

Integra NeuroSciences is recalling CODMAN Disposable Perforators 11mm and 9mm models due to inadequate welds that could lead to improper use. This recall expands the previous recall for size 14mm units. Read more at govinfonow.com/recall/51188-integra-neurosciences-recalls-codman-disposable-perforators-for-inadequate-welds.

Source Summary by GovInfoNow · govinfonow.com/recall/51188-integra-neurosciences-recalls-codman-disposable-perforators-for-inadequate-welds · Updated August 17, 2026 · FDA enforcement record: FDA #Z-0373-2026

Cite this page

“Integra NeuroSciences Recalls CODMAN Disposable Perforators for Inadequate Welds.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51188-integra-neurosciences-recalls-codman-disposable-perforators-for-inadequate-welds. Based on FDA recall #Z-0373-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0373-2026%22&limit=1).

Integra LifeSciences Corp. (NeuroSciences) is recalling CODMAN Disposable Perforators in sizes 11 mm and 9 mm due to inadequate welds, expanding a prior recall of size 14 mm units. The Food and Drug Administration announced the Class I voluntary recall on Sept. 26, 2025.

How to tell if you have it

Brand: Integra NeuroSciences
Product: CODMAN Disposable Perforator 11mm. Cranial Perforator; Model No. 261222; UDI: 10381780513612
Lot codes: 7221964 through 7221991, 7230624 through 7230651, 7282989 through 7283007, 7293432 through 7293448, 7293450, 7308709, 7308710, 7293449, 7293451, 7308706 through 7308715, 7322887 through 7322891, 7323305 through 7323309, 7332669 through 7332677, 7348757 through 7348782, 7371090 through 7371103, 7387974 through 7387987, 7387991, 7402327 through 7402334, 7406854 through 7406861, 7448431 through 7448434
Expiration dates: 2028-04-30 to 2029-07-31
Units affected: 16,251

The hazard

The recall addresses inadequate welds in the perforators. The expansion from size 14 mm to sizes 11 mm and 9 mm was conducted out of an abundance of caution.

Context

GovInfoNow's records show Integra LifeSciences Corp. (NeuroSciences) has 12 other recalls on record since April 4, 2025. Recent brand recalls include the June 5, 2026 OmniTract Surgical Retractor System recall for dry time issues and the April 10, 2026 Codman CerebroFlo EVD Catheter recall for endotoxin risk. Other recent recalls of similar products include the Jan. 13, 2026 Medtronic Octopus Nuvo Tissue Stabilizer recall for incorrect tube assembly and the Feb. 25, 2026 Olympus PKS Cutting Forceps recall for risk of jaw breaking.

How to tell if you have this one

Check for model numbers 261222, lot numbers listed in the description, and expiration dates between April 2028 and July 2029. The product is a cranial perforator used in surgery.

Brand
Integra NeuroSciences
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class I
Status
Ongoing
Distribution
Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Ecuador, France, French Guiana, Germany, Greece, India, Ireland, Italy, Japan, Jordan, Korea, Lithuania, Mexico, Morrocco, Netherlands, New Zealand, Palestine, State of, Philippines, Portugal, Puerto Rico, Qatar, Republic of North Macedonia, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan , Thailand, Trinidad and Tobago, Tunisia, Turkey, United Arab Emirates, United Kingdom of Great Britain and Northern Ireland, Vietnam.

Recall number	Product, codes & lots	Quantity
Z-0373-2026	CODMAN Disposable Perforator 11mm. Cranial Perforator.; Model No. 261222; UDI: 10381780513612; Lot No. 7221964, 7221972, 7221976, 7221977, 7221978, 7221979, 7221980, 7221981, 7221982, 7221983, 7221984, 7221985, 7221986, 7221987, 7221988, 7221989, 7221990, 7221991, 7230624, 7230625, 7230626, 7230627, 7230628, 7230629, 7230630, 7230631, 7230632, 7230633, 7230634, 7230635, 7230636, 7230637, 7230638, 7230639, 7230640, 7230641, 7230642, 7230643, 7230644, 7230645, 7230646, 7230647, 7230648, 7230649, 7230650, 7230651, 7230652, 7230653, 7230654, 7230655, 7230656, 7230657, 7230658, 7230659, 7230660, 7230661, 7282989, 7282990, 7282991, 7282992, 7282993, 7282994, 7282995, 7282996, 7282997, 7282998, 7282999, 7283000, 7283001, 7283002, 7283003, 7283004, 7283005, 7283006, 7283007, 7293432, 7293433, 7293434, 7293435, 7293436, 7293437, 7293438, 7293439, 7293440, 7293441, 7293442, 7293443, 7293444, 7293445, 7293446, 7293447, 7293448, 7293450, 7308709, 7308710, 7293449, 7293451, 7308706, 7308707, 7308708, 7308711, 7308712, 7308713, 7308714, 7308715, 7322887, 7322888, 7322889, 7322890, 7322891, 7323305, 7323306, 7323307, 7323308, 7323309, 7332669, 7332670, 7332671, 7332672, 7332673, 7332674, 7332675, 7332676, 7332677, 7348757, 7348758, 7348759, 7348760, 7348761, 7348762, 7348763, 7348764, 7348765, 7348766, 7348767, 7348768, 7348769, 7348770, 7348771, 7348772, 7348773, 7348774, 7348775, 7348776, 7348777, 7348778, 7348779, 7348780, 7348781, 7348782, 7371090, 7371091, 7371092, 7371093, 7371094, 7371095, 7371096, 7371097, 7371098, 7371099, 7371100, 7371101, 7371102, 7371103, 7387974, 7387975, 7387976, 7387977, 7387978, 7387979, 7387980, 7387981, 7387982, 7387983, 7387984, 7387985, 7387986, 7387987, 7387991, 7402327, 7402328, 7402329, 7402330, 7402331, 7402332, 7402333, 7402334, 7406854, 7406855, 7406856, 7406857, 7406858, 7406859, 7406860, 7406861, 7448431, 7448432, 7448433, 7448434; Expiration Date: 2028-04-30 to 2029-07-31.	16,251 units
Z-0374-2026	CODMAN Disposable Perforator 9mm. Cranial Perforator.; Model No. 261223; UDI: 10381780513605; Lot No. 5828553, 6264478, 6264481, 6264482, 7230672, 7230673, 7230674, 7230675, 7261971, 7268008, 7268009, 7268010, 7268011, 7268012, 7268013, 7268014, 7268015, 7268016, 7268017, 7268018, 7268019, 7282954, 7282955, 7293422, 7293423, 7293424, 7293425, 7293426, 7293427, 7293428, 7300667, 7300668, 7300669, 7300670, 7300672, 7300673, 7300674, 7371082, 7371083, 7379652, 7379922, 7379923, 7379924, 7379926, 7379928, 7379660, 7379925, 7379927, 7450559, 7450560, 7450561, 7450562, 7450563, 7450564, 7450565, 7450566, 7451273, 7451274, 7451275, 7451276, 7451277, 7451278, 7451279; Expiration Date: 2024-03-31 to 2029-07-31.	5,109 units

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for model number 261222 and lot numbers in the list provided in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Ecuador, France, French Guiana, Germany, Greece, India, Ireland,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 47 days after the firm started it.

Sep 26, 2025Firm started the recall
Nov 3, 2025FDA classified it Class I
Nov 12, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Do I need to stop using this product?

No action is required beyond checking if your product matches the affected details. The recall does not require immediate discontinuation.

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Link to this recall

<a href="https://govinfonow.com/recall/51188-integra-neurosciences-recalls-codman-disposable-perforators-for-inadequate-welds">Integra NeuroSciences Recalls CODMAN Disposable Perforators for Inadequate Welds (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0373-2026 (September 26, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0373-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.