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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96342

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

Open FDA event record

Event summary

Timeline bucket
March 12, 2025
Product types
Device
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
Draeger, 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

7 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 7

Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is intended for single use only. Component: Not applicable

Z-1493-2025
Recall number
Z-1493-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
65150 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP00355; UDI Number 04048675248996; All lot numbers

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

device · product 2 of 7

Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable

Z-1494-2025
Recall number
Z-1494-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
3325 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP01347; UDI Number 04048675249337; All lot numbers.

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

device · product 3 of 7

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable

Z-1495-2025
Recall number
Z-1495-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
3140

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP02737; UDI Number 04048675389620; All lot numbers.

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

device · product 4 of 7

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable

Z-1496-2025
Recall number
Z-1496-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
780 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP02738; UDI Number 04048675389637; All lot numbers.

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

device · product 5 of 7

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only

Z-1497-2025
Recall number
Z-1497-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
293660 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP02744; UDI Number 040486775389675; All lot numbers.

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

device · product 6 of 7

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only Component: Not applicable

Z-1498-2025
Recall number
Z-1498-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
9250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP02752; UDI Number 04048675389729; All lot numbers.

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

device · product 7 of 7

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only

Z-1499-2025
Recall number
Z-1499-2025
Initiated
March 12, 2025
Classification
Class I
Status
Ongoing
Recalling firm
Draeger, Inc.
Quantity
13620 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for cracks forming in the breathing circuit hose.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for cracks forming in the breathing circuit hose.

Code information

Model/Catalog Number: MP17103; UDI Number 04048675695660; All lot numbers.

Distribution pattern

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom