Carefusion 2200: Endoscopic Surgical Clamp May Crack Due to Manufacturing Issue
Carefusion 2200 recalls specific lots of their Diamond-Touch Bowel Clamp for potential rotation knob cracking from manufacturing adhesive issues. Affected units have UDI/DI 10885403160561 and Lot B23. Contact for remedy.
Use caution until it’s fixed
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Contact the company
What happened, in plain English
Carefusion 2200 is recalling specific lots of their Diamond-Touch Bowel Clamps that may crack due to a manufacturing adhesive issue. This could lead to the clamp failing during surgery, posing a risk to patients and surgical teams. Read more at govinfonow.com/recall/57650-carefusion-2200-endoscopic-surgical-clamp-may-crack-due-to-manufacturing.
Source Summary by GovInfoNow · govinfonow.com/recall/57650-carefusion-2200-endoscopic-surgical-clamp-may-crack-due-to-manufacturing · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2421-2023
Cite this page
“Carefusion 2200: Endoscopic Surgical Clamp May Crack Due to Manufacturing Issue.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57650-carefusion-2200-endoscopic-surgical-clamp-may-crack-due-to-manufacturing. Based on FDA recall #Z-2421-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2421-2023%22&limit=1).
Why it’s dangerous
The rotation knob on specific lots may crack or break because of an incorrect adhesive used during manufacturing. This could cause the clamp to malfunction during surgery, potentially leading to tissue damage or procedural failure.
Who’s affected
Surgical teams and hospitals using Carefusion 2200's Diamond-Touch Bowel Clamps with UDI/DI 10885403160561 and Lot B23 are most at risk. Patients undergoing endoscopic procedures with these clamps could face complications.
How to tell if you have this one
Check for the UDI/DI number 10885403160561 and Lot Number B23 on the clamp's packaging or label. This specific model is used in endoscopic surgical procedures.
- Brand
Carefusion 2200- Category
Medical device
All 15 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 II- Status
Ongoing- Distribution
US and Canada
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2415-2023 | Snowden-Pencer MIS DIAMOND-TOUCH GRASPER MCKERNAN FUNDUS 5MM, 32CM, RATCHETED, REF SP90-7012; endoscopic surgical device; UDI/DI 10885403159671, Lot Number B23 | 3 units |
| Z-2416-2023 | Snowden-Pencer MIS DIAMOND-TOUCH GRASPER DIAMOND JAW BABCOCK 5MM, 32CM, RATCHETED, REF SP90-7018; endoscopic surgical device; UDI/DI 10885403159701, Lot Number B23 | 3 units |
| Z-2417-2023 | Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device; UDI/DI 10885403159725, Lot Number B23 | 1 unit |
| Z-2418-2023 | Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM, 32CM, NON RATCHETED, REF SP90-7036; endoscopic surgical device; UDI/DI 10885403159862, Lot Number B23 | 0 units |
| Z-2419-2023 | Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7043; endoscopic surgical device; UDI/DI 10885403160547, Lot Numbers: L22, B23, C23 | 8 units |
| Z-2420-2023 | Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 35 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7044; endoscopic surgical device; UDI/DI 10885403160554, Lot Numbers: B23, C23 | 0 units |
| Z-2421-2023 | Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device; UDI/DI 10885403160561, Lot Number B23 | 2 units |
| Z-2422-2023 | Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device; UDI/DI 10885403160578, Lot Numbers: C23, L22 | 4 units |
| Z-2423-2023 | Snowden-Pencer MIS DIAMOND-TOUCH GRASPER CRILE CURVED JAW 5MM, 32CM, RATCHETED, REF SP90-7048; endoscopic surgical device; UDI/DI 10885403160592, Lot Number B23 | 0 units |
| Z-2424-2023 | Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 32CM, RATCHETED HANDLE, REF SP90-7066; endoscopic surgical device; UDI/DI 10885403160769, Lot Number B23 | 1 unit |
| Z-2425-2023 | Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7071; endoscopic surgical device; UDI/DI 10885403160790, Lot Numbers: L22, B23, C23 | 42 units |
| Z-2426-2023 | Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 45CM, RATCHETED, REF SP90-7220; endoscopic surgical device; UDI/DI 10885403161278, Lot Numbers: B23, C23 | 0 units |
| Z-2427-2023 | Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 45CM, RATCHETED, REF SP90-7243; endoscopic surgical device; UDI/DI 10885403161384, Lot Number B23 | 7 units |
| Z-2428-2023 | Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 45CM, RATCHETED HANDLE, REF SP90-7266; endoscopic surgical device; UDI/DI 10885403161513, Lot Numbers: B23, C23 | 1 unit |
| Z-2429-2023 | Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 45CM, RATCHETED, REF SP90-7271; endoscopic surgical device; UDI/DI 10885403161544, Lot Numbers: B23, C23 | 20 units |
What to do — step by step
Check Product Details
Verify the UDI/DI number 10885403160561 and Lot Number B23 on the clamp's packaging or label.
How this recall unfolded
Recall timeline
FDA published this recall 41 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-2421-2023 (July 13, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2421-2023 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.