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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80635

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

Open FDA event record

Event summary

Timeline bucket
July 06, 2018
Product types
Device
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Smiths Medical ASD 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

5 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 5

smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.

Z-0071-2019
Recall number
Z-0071-2019
Initiated
July 06, 2018
Classification
Class III
Status
Terminated
Recalling firm
Smiths Medical ASD Inc.
Quantity
12,000 devices

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labels are transposed

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.

Code information

Lot numbers 1703221A and 1705111A

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and WV. There was government distribution and no military distribution. Foreign distribution was made to Poland and Russia.

device · product 2 of 5

smiths medical portex First Breath Adult Nasal Cannula, REF 001285, Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.

Z-0072-2019
Recall number
Z-0072-2019
Initiated
July 06, 2018
Classification
Class III
Status
Terminated
Recalling firm
Smiths Medical ASD Inc.
Quantity
2,550 devices

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labels are transposed

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.

Code information

Lot number 1705151A

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and WV. There was government distribution and no military distribution. Foreign distribution was made to Poland and Russia.

device · product 3 of 5

smiths medical portex First Breath Adult Nasal Cannula, REF 001289, Curved Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients.

Z-0073-2019
Recall number
Z-0073-2019
Initiated
July 06, 2018
Classification
Class III
Status
Terminated
Recalling firm
Smiths Medical ASD Inc.
Quantity
3,000 devices

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labels are transposed

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.

Code information

Lot numbers 1703171A and 1705152A

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and WV. There was government distribution and no military distribution. Foreign distribution was made to Poland and Russia.

device · product 4 of 5

smiths medical portex First Breath Nasal Oxygen Cannula, REF 001292, with Gas Monitoring Line, 305 cm (10ft.) & Male Luer Connector, 213 cm (7ft.) Tubing, & Oxygen Adapter. Product Usage: For the administration of nasal oxygen and humidity to patients.

Z-0074-2019
Recall number
Z-0074-2019
Initiated
July 06, 2018
Classification
Class III
Status
Terminated
Recalling firm
Smiths Medical ASD Inc.
Quantity
13,750 devices

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labels are transposed

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.

Code information

Lot numbers 1702231A, 1703231A, and 1705163A

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and WV. There was government distribution and no military distribution. Foreign distribution was made to Poland and Russia.

device · product 5 of 5

smiths medical portex First Breath Nasal Oxygen Cannula, REF 001293, with Gas Monitoring Line, 305 cm (10ft.) & Female Luer Connector, 213 cm (7ft.) Tubing, & Oxygen Adapter. Product Usage: For the administration of nasal oxygen and humidity to patients.

Z-0075-2019
Recall number
Z-0075-2019
Initiated
July 06, 2018
Classification
Class III
Status
Terminated
Recalling firm
Smiths Medical ASD Inc.
Quantity
850 devices

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
labels are transposed

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

"Manufactured" and "Use By" labels are transposed incorrectly suggesting the product expires before it was manufactured.

Code information

Lot number 1705171A

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AR, CA, GA, IN, LA, OK, MA, MI, NC, NJ, NV, SC, TX, VA, and WV. There was government distribution and no military distribution. Foreign distribution was made to Poland and Russia.