ARROW IPN920364Recalls & reported problems
Teleflex Incorporated · Arrow-Trerotola(TM) PTD(R)* Set (Percutaneous Thrombolytic Device) · Class 2
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
12 other recalls cover devices cleared under the same FDA submission (K011056); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jan 11, 2022Terminated
The firm received reports indicating PTD tip separation during use.
Z-0629-2022 · Root cause: Process change control · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K011056. One submission often covers many models, so check the product and lot details in each record.
- Z-0626-2022 · Jan 11, 2022 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-65709-C, PT-03009, PT-65709-HS The Arrow-Trerotola Percutane
- Z-0625-2022 · Jan 11, 2022 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PT
- Z-0627-2022 · Jan 11, 2022 · TerminatedArrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) C
- Z-0624-2022 · Jan 11, 2022 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percuta
- Z-0623-2022 · Jan 11, 2022 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thro
- Z-0628-2022 · Jan 11, 2022 · Terminated5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-03000, PT-65509-S (PT-65509-S2 alternative), PT-01000-D (PT-010
- Z-0233-2022 · Sep 20, 2021 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-W The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in co
- Z-0231-2022 · Sep 20, 2021 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-12709-WC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in c
- Z-0234-2022 · Sep 20, 2021 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-WC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in c
- Z-0232-2022 · Sep 20, 2021 · TerminatedArrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-HFWC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in
- Z-1502-2009 · Feb 11, 2009 · TerminatedArrow OTW Percutaneous Thrombolytic Device (PTD) for fistulae and dialysis grafts
- Z-0842-05 · Mar 18, 2005 · TerminatedThe Arrow Trerotola Percutaneous Thrombolytic Device (Product Codes: PT-65709-WC, PT-65709-W, PT-65709-HFWC, and PT-12709-WC) consists of a catheter with an expandable fragmentati
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.