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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 84721

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

Open FDA event record

Event summary

Timeline bucket
January 13, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Stryker Instruments Div. of Stryker Corporation

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

3 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 3

SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332

Z-1097-2020
Recall number
Z-1097-2020
Initiated
January 13, 2020
Classification
Class II
Status
Terminated
Quantity
15150

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

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

Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

Code information

1921032

Distribution pattern

Domestic distribution nationwide. Foreign distribution to Netherlands and Australia.

device · product 2 of 3

Telescopic Smoke Evac Pencil, PB, Coated, Product No. SHKTSPCL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332

Z-1098-2020
Recall number
Z-1098-2020
Initiated
January 13, 2020
Classification
Class II
Status
Terminated
Quantity
15150

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

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

Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

Code information

1923011, 1923050, 1924004, 1924005, 1924015, 1929038, 1929039, 1929055

Distribution pattern

Domestic distribution nationwide. Foreign distribution to Netherlands and Australia.

device · product 3 of 3

Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332

Z-1099-2020
Recall number
Z-1099-2020
Initiated
January 13, 2020
Classification
Class II
Status
Terminated
Quantity
15150

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

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

Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

Code information

1922042, 1924003, 1929040, 1929048

Distribution pattern

Domestic distribution nationwide. Foreign distribution to Netherlands and Australia.