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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81874

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

Open FDA event record

Event summary

Timeline bucket
December 21, 2018
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Draeger Medical, Inc.

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

9 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 9

VentStar Basic 180, Catalog Number MP00349 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0736-2019
Recall number
Z-0736-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
325 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 2 of 9

VentStar Basic 250, Catalog Number MP00350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0737-2019
Recall number
Z-0737-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
170 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 3 of 9

VentStar Basic (P) 180, Catalog Number MP00351 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0738-2019
Recall number
Z-0738-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
525 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 4 of 9

VentStar Basic (P) 250, Catalog Number MP00352 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0739-2019
Recall number
Z-0739-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
75 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 5 of 9

VentStar Watertrap (P) 180, Catalog Number MP00361 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0740-2019
Recall number
Z-0740-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
25 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 6 of 9

VentStar Anesthesia WT(P) 180, Catalog Number MP00374 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0741-2019
Recall number
Z-0741-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
10 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 7 of 9

ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0742-2019
Recall number
Z-0742-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
25 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 8 of 9

ID Circuit Basic 250, Catalog Number MP01348 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0743-2019
Recall number
Z-0743-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
20 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

device · product 9 of 9

ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

Z-0744-2019
Recall number
Z-0744-2019
Initiated
December 21, 2018
Classification
Class I
Status
Terminated
Recalling firm
Draeger Medical, Inc.
Quantity
25 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

Code information

All Lots

Distribution pattern

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.