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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96849

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

Open FDA event record

Event summary

Timeline bucket
May 13, 2025
Product types
Device
Classifications
Class II
Statuses
Completed
Recalling firm wording
Cardinal Health 200, 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

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

SCD Comfort Knee Length Small, SKU 84021; Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller

Z-1917-2025
Recall number
Z-1917-2025
Initiated
May 13, 2025
Classification
Class II
Status
Completed
Recalling firm
Cardinal Health 200, LLC
Quantity
6517 cases total

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software logic may cause frequent E1 errors (system high pressure). Issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

Code information

UDI-DI (GTIN) 10885380186516 (EA) 50885380186514 (BX) ALL LOTS

Distribution pattern

Domestic US distribution to AK, CA, FL, MA, TX. International distribution to Japan.

device · product 2 of 3

Kendall SCD Comfort Sleeves Knee Length Small, Pediatric - For use with Kendall SCD SmartFlow, SKU 84021P Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller

Z-1918-2025
Recall number
Z-1918-2025
Initiated
May 13, 2025
Classification
Class II
Status
Completed
Recalling firm
Cardinal Health 200, LLC
Quantity
6517 cases total

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software logic may cause frequent E1 errors (system high pressure). Issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

Code information

UDI-DI (GTIN) 10885380197925 (EA) 50885380197923 (BX) ALL LOTS

Distribution pattern

Domestic US distribution to AK, CA, FL, MA, TX. International distribution to Japan.

device · product 3 of 3

Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD SmartFlow SKU 84021B Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Controller

Z-1919-2025
Recall number
Z-1919-2025
Initiated
May 13, 2025
Classification
Class II
Status
Completed
Recalling firm
Cardinal Health 200, LLC
Quantity
6517 cases total

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software logic may cause frequent E1 errors (system high pressure). Issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

Code information

UDI-DI (GTIN) 10885380186516 (EA) 50885380194687 (BX) ALL LOTS

Distribution pattern

Domestic US distribution to AK, CA, FL, MA, TX. International distribution to Japan.

Field note

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