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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 58185

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

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Event summary

Timeline bucket
March 01, 2011
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Terumo Cardiovascular Systems Corp

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

6 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 6

Terumo Custom Cardioplegia Delivery Set - Heat Exchanger Cardiopulmonary Bypass Item Numbers: 5852, 16010 Product Usage: This is a Cardioplegia Delivery System that is designed to delivery blood/solution to the patient undergoing cardiopulmonary bypass surgery. The set is designed to deliver blood/solutions at a 4:1 ratio. In includes a Conducer Heat Exchanger and a Bubble Trap module. Additionally, the set is constructed with a female luer connector that is the subject of the correction/removal activity

Z-0156-2015
Recall number
Z-0156-2015
Initiated
March 01, 2011
Classification
Class II
Status
Terminated
Quantity
596 units; 876 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line

Code information

Item Number: 58520-Lot Numbers: MF24, MM11, MN01. Manufacturing dates May 24, 20 I 0 through November I, 2010 Item Number: 1610-Lot Numbers: MM11, MN08, MNI5, MN29 MP07. Manufacturing dates October 11, 20 I 0 through December 7, 20 I 0

Distribution pattern

Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

device · product 2 of 6

Terumo Custom Integrated Cardioplegia Delivery Set-LINE FOR 15501/16015/5852 Item Number: 16110 Product Usage: This is a replacement line to multiple Cardioplegia Delivery Sets - and includes the female luer connector that is the subject of this correction/removal activity

Z-0157-2015
Recall number
Z-0157-2015
Initiated
March 01, 2011
Classification
Class II
Status
Terminated
Quantity
165 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

Code information

Lot Numbers: ML13, MM04. Manufacturing datese September 13, 2010 through October 4, 20 I 0.

Distribution pattern

Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

device · product 3 of 6

Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery.

Z-0158-2015
Recall number
Z-0158-2015
Initiated
March 01, 2011
Classification
Class II
Status
Terminated
Quantity
777 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

Code information

Lot Numbers: MN08, MNI5, MM11, MM18, MM25. Manufacturing dates October 1I, 2010 through Novemberl5, 20 I 0.

Distribution pattern

Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

device · product 4 of 6

Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes: Kits with a 5-digit code beginning with the digit 6: Catalog Number: 6XXXX ; Catalog Codes: Kits with a 5-digit code beginning with the digit 7: Catalog Number: 7XXXX Product usage: The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery. The Cardiovascular Procedure Kits are indicated for use only in the extracorporeal circuit for the cardiopulmonary bypass procedure(s) for which the user designed it.

Z-0159-2015
Recall number
Z-0159-2015
Initiated
March 01, 2011
Classification
Class II
Status
Terminated
Quantity
Catalog Number: 6XXXX: 4561 units; Catalog Number: 7xxxx : 19356 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line.

Code information

Catalog Number: 6XXXX Lot Numbers: ML07, MM18, MM25, MN08, MN IS, MN22. Manufacturing dates September 7, 20 I 0 through November 22, 20 I 0. Catalog Number: 7XXXX Lot Numbers: ML07,ML20, MM18, MM25, MNO1, MN08, MN15, MN29,MP06, MP13. Manufacturing dates September 7, 2010 through December 13,2010.

Distribution pattern

Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

device · product 5 of 6

Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog Number: 6375 Product Usage: Cardioplegia Delivery System that is designed to delivery blood/solution to the patient undergoing cardiopulmonary bypass surgery. The set is designed to deliver blood/solutions at a 4: I ratio. Includes a Conducer Heat Exchanger and a MP4 Temperature & Pressure Module. Additionally, the set is constructed with a female luer connector that is the subject of the correction/removal activity.

Z-0160-2015
Recall number
Z-0160-2015
Initiated
March 01, 2011
Classification
Class II
Status
Terminated
Quantity
Catalog: 16579 ; Catalog 6375: 3256 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Defect in the luer connector can compromise the seal on the female side of the connector. and the compromised seal can introduce air in the table line

Code information

Catalog Number: 165720 Lot Numbers: MDI5, MD15B, MD22, ME19, MP13. Manufacturing dates March 15, 20 I 0 through December 13, 20 I 0. Catalog Number: 6375 Lot Numbers: MD15, ME19, MPI3 Manufacturing dates March 15, 2010 through December 13, 20 I 0

Distribution pattern

Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.

device · product 6 of 6

Terumo Custom Cardioplegia Delivery Sets Catalog Code: 204880 Product Usage: This is a replacement line to multiple Cardioplegia Delivery Sets-and includes the female luer connector" that is the subject of this correction/removal activity

Z-0161-2015
Recall number
Z-0161-2015
Initiated
March 01, 2011
Classification
Class II
Status
Terminated
Quantity
24 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Defect in the luer connector can compromise the seal on the female side of the connector and the compromised seal can introduce air in the table line

Code information

Lot Numbers: MN08 Manufacturing Date November 8, 20 I 0.

Distribution pattern

Worldwide Distribution: US (nationwide) and the countries of Canada, Brazil, Hong Kong, Korea, and Thailand.