Lower riskMedical device recall · FDA · Published August 7, 2019
Integra Jarit GEMINI CLAMP 9 1/4 inch recall: corrosion risk after cleaning
Integra recalls 9 1/4 inch GEMINI CLAMP for possible corrosion after multiple sterilizations, requiring replacement to prevent breakage during medical procedures.
A small crack at the box lock corner may after multiple cleaning and sterilization cycles produce an increased risk of corrosion, weakening the instrument and resulting in premature need for replacement and/or breakage of the instrument
Take action
Contact the company
📍Recalling firmIntegra LifeSciences Corp.311 Enterprise Dr · Plainsboro, NJ 08536-3344
✎ GovInfoNow plain-language explainer
Integra is recalling its 9 1:4 inch GEMINI CLAMP used in vascular procedures due to a crack risk after repeated cleaning that could cause breakage. This affects medical devices used in surgeries and requires replacement to avoid instrument failure. Read more at govinfonow.com/recall/67250-integra-jarit-gemini-clamp-9-1-4-inch-recall-corrosion.
“Integra Jarit GEMINI CLAMP 9 1/4 inch recall: corrosion risk after cleaning.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67250-integra-jarit-gemini-clamp-9-1-4-inch-recall-corrosion. Based on FDA recall #Z-2435-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2435-2019%22&limit=1).
Integra LifeSciences Corp. recalled the Integra Jarit GEMINI CLAMP 9 1/4 inch on Aug. 7, 2019, according to the FDA. The Class II device may crack after sterilization cycles, posing a risk of breakage during vascular and cardiothoracic procedures.
How to tell if you have it
Brand: Integra
Product: Integra Jarit GEMINI CLAMP 9 1/4 inch
Cat. #: 140-332
Lot #: AA1901
The hazard
A small crack at the box lock corner may produce an increased risk of corrosion after multiple cleaning and sterilization cycles. This weakening can result in the premature need for replacement and/or breakage of the instrument.
Context
GovInfoNow's records show Integra LifeSciences Corp. has 35 other recalls on record since Aug. 18, 2017. Recent brand recalls include the Integra AURORA Surgiscope System (Feb. 6, 2025), MediHoney Wound Dressing Gel (Jan. 10, 2025), and CODMAN CERTAS Plus Valve (Dec. 16, 2024). Other recent recalls of similar products include Stryker Hoffmann II Connecting Rod Micro 3 x 50mm (July 1, 2026) and Penumbra RED 62 Reperfusion Catheter (July 24, 2026).
How to tell if you have this one
Check for the model 'Jarit GEMINI CLAMP 9 1/4 inch' with catalog number 140-332 and lot number AA1901. The product is used in vascular and cardiothoracic surgeries.
Brand
Integra
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check for Recalled Model
Look for the model name 'Jarit GEMINI CLAMP 9 1/4 inch' with catalog number 140-332 and lot number AA1901.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-2435-2019 (August 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2435-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.