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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86808

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

Open FDA event record

Event summary

Timeline bucket
February 18, 2021
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Smisson-Cartledge Biomedical, 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

ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion System, used for infusion of: -crystalloid, colloid, or blood product, including packed red blood cells, as volume replacement for patients suffering from blood loss due to trauma or surgery -warmed fluid to rewarm patients after surgery or hypothermia -warmed fluid for irrigation in urology procedures

Z-1258-2021
Recall number
Z-1258-2021
Initiated
February 18, 2021
Classification
Class I
Status
Terminated
Quantity
18482 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

Code information

Model PTC-1200, GTIN (01)00857893006059, all serial numbers

Distribution pattern

Nationwide Distribution in US and international via 2 US distributors (VA and GA)

device · product 2 of 3

ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion System, used for infusion of: -crystalloid, colloid, or blood product, including packed red blood cells, as volume replacement for patients suffering from blood loss due to trauma or surgery -warmed fluid to rewarm patients after surgery or hypothermia -warmed fluid for irrigation in urology procedures

Z-1259-2021
Recall number
Z-1259-2021
Initiated
February 18, 2021
Classification
Class I
Status
Terminated
Quantity
7118 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

Code information

Model DNC-1200, GTIN # (01) 00857893006073, all serial numbers

Distribution pattern

Nationwide Distribution in US and international via 2 US distributors (VA and GA)

device · product 3 of 3

ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion System, used for infusion of: -crystalloid, colloid, or blood product, including packed red blood cells, as volume replacement for patients suffering from blood loss due to trauma or surgery -warmed fluid to rewarm patients after surgery or hypothermia -warmed fluid for irrigation in urology procedures

Z-1260-2021
Recall number
Z-1260-2021
Initiated
February 18, 2021
Classification
Class I
Status
Terminated
Quantity
11768 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customers are being notified of results from a Toxicological Risk Assessment related to potential for aluminum ions to leach into warmed fluids.

Code information

Model PNC-1200, GTIN # (01) 00857893006066, all serial numbers

Distribution pattern

Nationwide Distribution in US and international via 2 US distributors (VA and GA)