PlainRecalls

Stryker Instruments Div. of Stryker Corporation

Compiled from official public sources by the publisher.

161 recalls on record · Latest: Jul 27, 2022

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Agency notice ledger

Federal filing book Stryker Instruments Div. HEAVY-BOOK · SINGLE-AGENCY

#99 of 14,151 · 161 notices · 0.154% archive

  • BOOK 161 notices
  • RANK #99 of 14,151
  • SHARE 0.154% archive
  • AGENCY FDA Devices (161)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 27, 2022
  • PHOTO Audi

Nearest notice-volume peer: Audi (1 notice gap)

Stryker Instruments Div. of Stryker Corporation accounts for about 0.154% of the 104,423-notice archive on 161 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 →

Where Stryker Instruments Div. sits among 14,151 recalling firms

Stryker Instruments Div. of Stryker Corporation ranks 99th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Stryker Instruments Div. vs all firms by recall-notice count

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

161 99th of 14151 higher than 14,052 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 Instruments Div. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Stryker Instruments Div. of Stryker Corporation holds about 0.154% of archive notices alongside 161 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 12, 2013

Stryker Instruments 0400-820-000S3 T4 Toga w/Inside Shoulder Ties, Sterile, O; single use; Product Usage: Protection System and are intended to protect the patient, healthcare personnel and operating room personnel against contamination, exposure of infectious bodily fluids, and the transfer of microorganismsand particulate material.
FDA Devices Moderate Dec 12, 2012

Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A REF 0702-001-000, Rx, Caution, consult accompanying documents Consult instructions for use, Max Vacuum; 21.0 in-Hg, 530 mm-Hg, The Neptune Waste Management System consists of a mobile rover unit used to suction and collect fluid waste, small debris and electrocautery smoke from a surgical site. Mobility allows the rover unit to be relocated to a waste disposal area where the rovers collection canisters can be emptied, via the docking station.

FDA Devices Moderate Dec 12, 2012

Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A REF 0702-002-000, Rx Caution, consult accompanying documents Consult instructions for use, Max Vacuum; 21.0 in-Hg, 530 mm-Hg, The Neptune Waste Management System consists of a mobile rover unit used to suction and collect fluid waste, small debris and electrocautery smoke from a surgical site. Mobility allows the rover unit to be relocated to a waste disposal area where the rovers collection canisters can be emptied, via the docking station.

FDA Devices Critical Aug 22, 2012

Neptune 1 Silver Rover, Part 0700-003-000 Stryker Instruments Neptune Rover IFU part 0700-001-700
FDA Devices Critical Aug 22, 2012

Neptune Rover Waste Management System, Neptune 2 Ultra Intended for use in the surgical environment or physician's office to collect and dispose of surgical fluid waste.
FDA Devices Critical Aug 22, 2012

Stryker Neptune Bronze Rover, Part 0700-007-000 Neptune Bronze Rover Waste Management System Instructions For Use. Intended for use in the surgical environment or physician's office to collect and dispose of surgical fluid waste.
FDA Devices Critical Aug 22, 2012

Neptune 1 Gold Rover (120 Vand 230V ) Waste Management System Part Number 0700-001-000, 0700-002-000(International) Instructions For Use 0700-001-700, 0700-002-707 Intended for use in the surgical environment or physician's office to collect and dispose of surgical fluid waste.
FDA Devices Moderate Aug 8, 2012

RF Cannula, 100 mm,Curved 10 MM, 20 G, REF 0406-630-125 RX only, Disposable ( 10/pk) Product Usage: The Stryker RF Cannulae, in combination with the Stryker RF Generator/Multi- Gen and electrodes, are intended for coagulation of soft tissue in orthopedic, arthroscopic, spinal, and neurosurgical applications.
FDA Devices Moderate Aug 8, 2012

RF Cannula, 100 mm,Curved 5 MM, 20 G, REF 0406-630-115 RX only, Disposable ( 10/pk) Product Usage: The Stryker RF Cannulae, in combination with the Stryker RF Generator/Multi- Gen and electrodes, are intended for coagulation of soft tissue in orthopedic, arthroscopic, spinal, and neurosurgical applications.
FDA Devices Moderate Jun 20, 2012

T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the members of the surgical team in order to help protect against contamination and/or exposure of infectious body fluids and harmful microorganisms.
FDA Devices Moderate Jun 20, 2012

T4-Hytrel Zipper Toga Product Usage - The togas are intended to provide a barrier between the operating room and the members of the surgical team in order to help protect against contamination and/or exposure of infectious body fluids and harmful microorganisms.

Stryker Instruments Div. carries an outsized archive share

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

Frequently Asked Questions

How many federal recall notices name Stryker Instruments Div.? ▼
PlainRecalls indexes 161 distinct federal recall events naming Stryker Instruments Div. of Stryker Corporation, 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 Instruments Div. sit among other recalling firms? ▼
Stryker Instruments Div. of Stryker Corporation ranks #99 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Stryker Instruments Div.'s notices? ▼
FDA Devices accounts for 161 of this firm's 161 indexed notices.
What product category dominates Stryker Instruments Div.'s filing book? ▼
Filings for Stryker Instruments Div. of Stryker Corporation 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 Instruments Div. of Stryker Corporation: 161 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 Instruments Div. of Stryker Corporation; individual notices remain authoritative on each linked recall page.

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