Stradis Healthcare NARMD Medical Depot Forceps Recall: Sterile Barrier Compromised
Stradis Healthcare recalls Kelly Straight 5.5" forceps (part ZZ-0700) due to potential sterile barrier compromise. Affected lots: 22145487092 and 22154486659. No remedy specified in recall notice.
Recall notice
The sterile barrier may be compromised.
Contact the company
What happened, in plain English
Stradis Healthcare is recalling Kelly Straight 5.5" medical forceps (part number ZZ-0700) because the sterile barrier might be compromised. This could lead to infections during medical procedures if the forceps are used without proper sterility. Read more at govinfonow.com/recall/60313-stradis-healthcare-narmd-medical-depot-forceps-recall-sterile-barrier-compromised.
Source Summary by GovInfoNow · govinfonow.com/recall/60313-stradis-healthcare-narmd-medical-depot-forceps-recall-sterile-barrier-compromised · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1553-2022
Cite this page
“Stradis Healthcare NARMD Medical Depot Forceps Recall: Sterile Barrier Compromised.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60313-stradis-healthcare-narmd-medical-depot-forceps-recall-sterile-barrier-compromised. Based on FDA recall #Z-1553-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1553-2022%22&limit=1).
Why it’s dangerous
The sterile barrier might not be fully intact, which could allow contamination during medical procedures. If the forceps are used without proper sterility, this could lead to infections in patients.
Who’s affected
Medical professionals using these forceps for procedures are most at risk. Patients receiving procedures with compromised sterile barriers could face infections.
How to tell if you have this one
Check for the part number ZZ-0700 on the forceps. Affected lots are 22145487092 and 22154486659. These forceps were sold with the UDI/DI code M752ZZ07000.
- Brand
Stradis Healthcare- Category
Medical device
All 3 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 Nationwide distribution in the state of SC.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1552-2022 | NARMD MEDICAL DEPOT Scissors Iris Curved 4.5", Part Number ZZ-0697; SKU/Part Number: ZZ-0697; Lots: 22026482044 and 22152487922 UDI/DI: M752ZZ06970 | 50 units |
| Z-1553-2022 | NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700; SKU/Part Number: ZZ-0700; Lots: 22145487092 and 22154486659 UDI/DI: M752ZZ07000 | 825 units |
| Z-1554-2022 | NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701; SKU/Part Number: ZZ-0701; Lots: 22027483172 and 22131487071 UDI/DI: M752ZZ07010 | 850 units |
What to do — step by step
Check Product Details
Look for part number ZZ-0700 and affected lots 22145487092 or 22154486659 on the forceps.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of SC.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 30 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-1553-2022 (July 25, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1553-2022 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.