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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85996

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

Open FDA event record

Event summary

Timeline bucket
July 06, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
TELEFLEX 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

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

Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2726-2020
Recall number
Z-2726-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
75320 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1811421 1812421 1901421 1904421 1905421 1906421 1907421 1908421 1909421

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

device · product 2 of 7

Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2727-2020
Recall number
Z-2727-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
27341 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1812431 1901431 1902431 1903431 1904431 1905431 1906431 1907431 1908431 1909431

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

device · product 3 of 7

Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2728-2020
Recall number
Z-2728-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
7401 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1812441 1901441 1903441 1905441 1906441 1907441 1909441

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

device · product 4 of 7

Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2729-2020
Recall number
Z-2729-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
20600 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1906321 1907321 1908321 1909321

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

device · product 5 of 7

Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2730-2020
Recall number
Z-2730-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
301085 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1812331 1901331 1903331 1905331 1906331 1907331 1908331 1909331

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

device · product 6 of 7

Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2731-2020
Recall number
Z-2731-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
350779 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1811341 1901341 1902341 1904341 1905341 1906341 1907341 1908341 1909341

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

device · product 7 of 7

Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Z-2732-2020
Recall number
Z-2732-2020
Initiated
July 06, 2020
Classification
Class II
Status
Terminated
Recalling firm
TELEFLEX MEDICAL INC
Quantity
29740 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Breaking at the point of a welded joint

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Breaking at the point of a welded joint

Code information

Lot/Batch Numbers: 1811351 1812351 1901351 1903351 1904351 1905351 1906351 1907351 1908351 1909351

Distribution pattern

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

Field note

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