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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90492

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

Open FDA event record

Event summary

Timeline bucket
June 03, 2022
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
ROi CPS LLC

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

2 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 2

Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV00214Q - CV.

Z-1407-2022
Recall number
Z-1407-2022
Initiated
June 03, 2022
Classification
Class II
Status
Terminated
Recalling firm
ROi CPS LLC
Quantity
86 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.

Code information

(1) Item #830099008 - Lot #92534, exp. 11/13/2022, UDI #10194717114895; (2) Item #830019017 - Lot #92612, exp. 8/31/2023, UDI #10194717113249.

Distribution pattern

Distribution was made to MO. There was no foreign/military/government distribution.

device · product 2 of 2

Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.

Z-1408-2022
Recall number
Z-1408-2022
Initiated
June 03, 2022
Classification
Class II
Status
Terminated
Recalling firm
ROi CPS LLC
Quantity
40 kits

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.

Code information

Lot #92605, exp. 8/31/2023, Item #830014016, UDI #10194717110156.

Distribution pattern

Distribution was made to MO. There was no foreign/military/government distribution.