CLASS II ONGOING Device recall · Reported 24 Aug 2022 · FDA Enforcement Report
Narmd Medical Depot Forceps - Kelly Curved 5.5" recalled
Stradis Medical is recalling Narmd Medical Depot Forceps - Kelly Curved 5.5", distributed nationwide in the US. The recall was initiated on 25 Jul 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1554-2022
- FDA event ID
- 90668
- Recalling firm
- Stradis Medical, Peachtree Corners, GA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 25 Jul 2022
- FDA classified
- 18 Aug 2022
- Reported
- 24 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Sterility
- Device type
- Surgical Instruments
Timeline
| 25 Jul 2022 | Recall initiated by company | |
| 18 Aug 2022 | Classified by FDA | +24 days |
| 24 Aug 2022 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The sterile barrier may be compromised.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701
Where it was distributed
US Nationwide distribution in the state of SC.
Questions about this recall
Why was it recalled?
The sterile barrier may be compromised.
Which lots are affected?
SKU/Part Number: ZZ-0701; Lots: 22027483172 and 22131487071 UDI/DI: M752ZZ07010
Where was it sold?
US Nationwide distribution in the state of SC.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 90668This product is part of a recall event; the main page for the event is Narmd Medical Depot Forceps - Kelly Straight 5.5" recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Narmd Medical Depot Forceps - Kelly Straight 5.5" recalled | Stradis Medical | Sterility | Nationwide | |
| CLASS II | Narmd Medical Depot Scissors Iris Curved 4.5" recalled | Stradis Medical | Sterility | Nationwide |
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