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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 88669

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

Open FDA event record

Event summary

Timeline bucket
September 01, 2021
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Flower Orthopedics 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

4 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 4

Flower Drill Bit Kit 2.0 mm - intended to be used with solid 2.0mm screws and can be used with any plate that has been cleared as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. mechanism. Catalog Number: DBK 020 2013002721

Z-0111-2022
Recall number
Z-0111-2022
Initiated
September 01, 2021
Classification
Class II
Status
Terminated
Quantity
2 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

Code information

Lot Number: 2013002721, 2013003589 Unique Identifier: 00840118101264

Distribution pattern

Arizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas Virginia

device · product 2 of 4

Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with any plate as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. Catalog Number: DBK 024

Z-0112-2022
Recall number
Z-0112-2022
Initiated
September 01, 2021
Classification
Class II
Status
Terminated
Quantity
33 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

Code information

Lot Number: 2101321194 Unique Identifier: 00840118101288

Distribution pattern

Arizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas Virginia

device · product 3 of 4

Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with solid 2.7mm screws and can be used with any the Flower Small and Medium Implant Set Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set or Flower Upper Extremity Plating Set and uses the medium locking mechanism. Catalog Number: DBK 027

Z-0113-2022
Recall number
Z-0113-2022
Initiated
September 01, 2021
Classification
Class II
Status
Terminated
Quantity
3 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

Code information

Lot Number: 2013003588, 2013004613 Unique Identifier: 00840118101295

Distribution pattern

Arizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas Virginia

device · product 4 of 4

Flower Lag Screw Kit 2.7 mm-intended to be used with 2.7mm lag screws and can be used with any plate that as part of the Flower Small and Medium Implant Set, Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set , or Flower Upper Extremity Plating Set and uses the medium locking mechanism. Catalog Number: LSK 027

Z-0114-2022
Recall number
Z-0114-2022
Initiated
September 01, 2021
Classification
Class II
Status
Terminated
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

Code information

Lot Number: 2013003419 Unique Identifier: 00840118103688

Distribution pattern

Arizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas Virginia