Stryker Sustainability Solutions
Stryker Sustainability Solutions holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2026, with 65 FDA device recalls on record.
Top product codes for Stryker Sustainability Solutions
FDA recalls by Stryker Sustainability Solutions
10 most recent of 65- Z-2177-2026 — BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
- Z-2174-2026 — BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2191-2026 — Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2181-2026 — BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2187-2026 — Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2195-2026 — Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2176-2026 — BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2192-2026 — Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2198-2026 — Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Z-2185-2026 — CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Stryker Sustainability Solutions
- K260636 — Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating
- K250898 — Reprocessed HARMONIC 700 Shears (3 models)
- K241758 — Reprocessed RD SET Adt Pulse Oximeter Sensor (4000) +3 more
- K241606 — Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm Length (HAR1120) +1 more
- K233471 — Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm length (HAR1120) +1 more
- K231621 — Reprocessed ViewFlex Xtra ICE Catheter (D087031)
- K230251 — Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
- K230255 — Remanufactured LigaSure Exact Dissector Without Nano-coating LF2019
- K222019 — Reprocessed RD SET Adt Pulse Oximeter Sensor (4000), Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001), Reprocessed RD SET Inf Pulse Oximeter Sensor (4002), Reprocessed RD SET Adt Pulse Oximeter Sensor (4003)
- K220481 — Remanufactured LigaSure Exact Dissector, Without Nano-coating (LF2019)
- K220411 — Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
- K211138 — Reprocessed Pulse Oximeter Sensor (D-25), Reprocessed Pulse Oximeter Sensor (D-25L), Reprocessed Pulse Oximeter Sensor (D-20), Reprocessed Pulse Oximeter Sensor (N-25), Reprocessed Pulse Oximeter Sensor (I-20), Reprocessed Pulse Oximeter Sensor (Max-A), Reprocessed Pulse Oximeter Sensor (Max-AL), Reprocessed Pulse Oximeter Sensor (Max-P), Reprocessed Pulse Oximeter Sensor (Max-N), Reprocessed Pulse Oximeter Sensor (Max-I)
- K211140 — Reprocessed Masimo Pulse Oximeter (1859 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (1860 Pediatric O2 Transducer), Reprocessed Masimo Pulse Oximeter (1861 Infant O2 Transducer), Reprocessed Masimo Pulse Oximeter (1862 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (2317 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (2319 Infant O2 Transducer), Reprocessed Masimo Pulse Oximeter (2320 Adult O2 Transducer), Reprocessed Masimo Pulse Oximeter (2328 Infant O2
- K202554 — Reprocessed HARMONIC ACE+ 7, 5 mm Diameter Shears with Advanced Hemostasis
- K201756 — Reprocessed MyoSure Tissue Removal Device, Reprocessed MyoSure REACH Tissue Removal Device, Reprocessed MyoSure LITE Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device, Reprocessed MyoSure XL Tissue Removal Device for Fluent
- K201511 — Reprocessed Endoscopic Trocars and Sleeves
- K200205 — Reprocessed Advisor FL Circular Mapping Catheter, Sensor Enabled
- K182238 — Reprocessed ViewFlex Xtra ICE Catheter
- K181056 — Reprocessed CS Diagnostic Electrophysiology Catheter
- K180499 — Reprocessed LigaSure Maryland Jaw Sealer/Divider
- K180451 — Reprocessed LigaSure Impact without Nano-coating Large Jaw, Open Sealer/Divider
- K172856 — Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider
- K170456 — Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology
- K161693 — Reprocessed HARMONIC ACE+7, 5 mm Diameter Shears with Advanced Hemostasis
- K153415 — Reprocessed Stryker External Fixation Devices
- K150538 — Reprocessed LigaSure ImpactTM Curved, Large Jaw, Open Sealer/Divider
- K133672 — REPROCESSED HARMONIC ACE SHEARS WITHOUT ADAPTIVE TISSUE TECHNOLOGY
- K133578 — REPROCESSED LIGASURE BLUNT TIP LAPAROSCOPIC SEALER/DIVIDER
- K132629 — REPROCESSED DILATING TIP TROCARS
- K121855 — RESPROCESSED SERFAS ENERGY PROBE
- K112292 — REPROCESSED 2515 NAV VARIABLE ELECTROPHYSIOLOGY CATHETER
- K112232 — REPROCESSED ELECTROPHYSIOLOGY CATHETERS
Data sourced from openFDA. This site is unofficial and independent of the FDA.