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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90668

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 25, 2022
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Stradis Medical, LLC dba Stradis Healthcare

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

NARMD MEDICAL DEPOT Scissors Iris Curved 4.5", Part Number ZZ-0697

Z-1552-2022
Recall number
Z-1552-2022
Initiated
July 25, 2022
Classification
Class II
Status
Ongoing
Quantity
50 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
sterile barrier may be compromised

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The sterile barrier may be compromised.

Code information

SKU/Part Number: ZZ-0697; Lots: 22026482044 and 22152487922 UDI/DI: M752ZZ06970

Distribution pattern

US Nationwide distribution in the state of SC.

device · product 2 of 3

NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700

Z-1553-2022
Recall number
Z-1553-2022
Initiated
July 25, 2022
Classification
Class II
Status
Ongoing
Quantity
825 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
sterile barrier may be compromised

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The sterile barrier may be compromised.

Code information

SKU/Part Number: ZZ-0700; Lots: 22145487092 and 22154486659 UDI/DI: M752ZZ07000

Distribution pattern

US Nationwide distribution in the state of SC.

device · product 3 of 3

NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701

Z-1554-2022
Recall number
Z-1554-2022
Initiated
July 25, 2022
Classification
Class II
Status
Ongoing
Quantity
850 units

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
sterile barrier may be compromised

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The sterile barrier may be compromised.

Code information

SKU/Part Number: ZZ-0701; Lots: 22027483172 and 22131487071 UDI/DI: M752ZZ07010

Distribution pattern

US Nationwide distribution in the state of SC.