PlainRecalls

Stryker Sustainability Solutions

Compiled from official public sources by the publisher.

65 recalls on record · Latest: May 20, 2026

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Agency notice ledger

Federal filing book Stryker Sustainability Solu… MID-BOOK · SINGLE-AGENCY

#279 of 14,151 · 65 notices · 0.062% archive

  • BOOK 65 notices
  • RANK #279 of 14,151
  • SHARE 0.062% archive
  • AGENCY FDA Devices (65)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 20, 2026
  • PHOTO Health Innovations Ph…

Nearest notice-volume peer: Health Innovations Pharmacy, Inc (0 notice gap)

Stryker Sustainability Solutions accounts for about 0.062% of the 104,423-notice archive on 65 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Stryker Sustainability Solu… compares to 14,151 recalling firms

Stryker Sustainability Solutions ranks 279th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Stryker Sustainability Solu… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

65 279th of 14151 higher than 13,869 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Stryker Sustainability Solu… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Stryker Sustainability Solutions holds about 0.062% of archive notices alongside 65 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 16, 2016

Reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Model Numbers: 401940, 402004 UPC Code: 00885825007409 00885825007744 Diagnostic electrophysiology (EP) catheters are specially designed electrode catheters that transmit electrical impulses and can be positioned for endocardial recording or stimulation. Diagnostic EP catheters incorporate a handpiece, a flexible shaft and a distal tip section containing diagnostic electrodes. Reprocess
FDA Devices Moderate Nov 9, 2016

Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or dual-bladder inflatable cuffs connected to a tourniquet system via a hose assembly. When wrapped around a limb and inflated, tourniquet cuffs apply an adequate amount of pressure on the arterial blood flow in a limb to create a bloodless surgical field. Tourniquet cuffs are available in a variety of sizes to accommodate a wide range of limb circumferences.
FDA Devices Critical Jul 27, 2016

AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
FDA Devices Moderate Jun 1, 2016

Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters; Model #: 401450, 401877. Indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.
FDA Devices Moderate May 18, 2016

Mallinckrodt Evac Tracheal Tubes Model #124170-MALLINCKRODT & 124175
FDA Devices Moderate May 18, 2016

Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
FDA Devices Moderate Jan 20, 2016

Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Cuffs Model Numbers: 5921-218-135, 5921-044-135, 5921-034-135, 5921-034-235, 5921-024-236 Indicated for use in patients who require surgery of the extremities.
FDA Devices Critical Jan 13, 2016

The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman Pleural/Pneumopericardial Drainage Set consists of pigtail catheter, access needle, dilator, and wire guide. The set also includes a multipurpose tubing adapter, and three-way stopcock.
FDA Devices Moderate Nov 18, 2015

SSS Reprocessed Zimmer, Synthes, Stryker and Linvatec Drill Bits and Blades Surgical drill bits, blades, burs, chisels, rasps, taps and reamers are specially designed surgical accessories to help the surgeon cut and drill bone and bony structures. Reprocessed surgical accessories are indicated for use in patients requiring surgery involving bone and bony structures.
FDA Devices Moderate Sep 2, 2015

Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery, Inc. Excel Trocar Sleeve w/Stability Sleeve 5mm x 100mm Reprocessed by Stryker Sustainability Solutions Product Usage: The Reprocessed Ethicon ENDOPATH¿ XCEL Universal Trocar Stability Sleeve is a sterile single patient use device with a radiolucent sleeve. The trocar sleeve contains two seals that accommodate instruments 5mm in diameter. Together, these two seals minimize gas leakage when instruments are inserted or withdr
FDA Devices Moderate Jul 1, 2015

Cannula and Seal; 5mm x 100mm and 12mm x 100mm Model #: CTS02 and CTS22. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.
FDA Devices Moderate Jul 1, 2015

Optical Access System; 5mm x 100mm and 12mm x 100mm; Model #: CTR03 and CTR73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.
FDA Devices Moderate Jul 1, 2015

Fios First Entry; 5mm x 100mm and 12mm x 100mm; Model #:CTF03 and CTF73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.
FDA Devices Moderate Nov 27, 2013

Reprocessed Diagnostic Electrophysiology (EP) Catheters and Diagnostic EP Catheter Cables, Model Numbers: D6-DR-252-RT, F6-QF-252RT, 201101, 201104, 401442, 401860, D7-A20-131-RT, 401661, 401972, 401977, 401981, 401982, C6-MR/MST4-SA, CB3434CT. Product Usage: Reprocessed diagnostic EP catheters are indicated for temporary intracardiac sensing, recording, stimulation and electrophysiological mapping of cardiac structures. Note: These devices do not support or sustain life. Diagnostic EP Cat
FDA Devices Moderate Feb 27, 2013

STRYKER Sustainability Solutions, AC Power Adaptor for Restep Deep Vein Thrombosis (DVT) System, an external compression system. PUMPKIT (Pump Kit), and RSP159-01 (AC Power Adaptor).

Stryker Sustainability Solu… carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Philips Medical Systems, Inc. 65 Waldemar Link GmbH & Co. Kg (Mfg Site) 65 Microbiologics Inc 66 Nobel Biocare Usa Llc 66

Frequently Asked Questions

How many federal recall notices name Stryker Sustainability Solu…? ▼
PlainRecalls indexes 65 distinct federal recall events naming Stryker Sustainability Solutions, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Stryker Sustainability Solu… sit among other recalling firms? ▼
Stryker Sustainability Solutions ranks #279 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Stryker Sustainability Solu…'s notices? ▼
FDA Devices accounts for 65 of this firm's 65 indexed notices.
What product category dominates Stryker Sustainability Solu…'s filing book? ▼
Filings for Stryker Sustainability Solutions span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Stryker Sustainability Solutions: 65 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Stryker Sustainability Solutions; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026