Champion SlingShot CAT02855Recalls & reported problems
Stryker Corporation · CHAMPION SLINGSHOT 45 RIGHT · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327123692), received between Jul 29, 2019 and Apr 21, 2026 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Expiration Date Error” (3 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Expiration Date Error3
- Break1
- Material Fragmentation1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Device Embedded In Tissue or Plaque1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 21, 2026Expiration Date Error
IT WAS REPORTED THAT THE REP HAD OPENED THE ITEM AND REALIZED THEY WERE EXPIRED. HE DID NOT LET THE SURGEON USE THEM. THESE PRODUCT WENT DOWN AS WASTE AND NEVER TOUCHED THE STERILE FIELD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24947852 ↗MalfunctionApr 21, 2026Expiration Date Error
IT WAS REPORTED THAT THE REP HAD OPENED THE ITEM AND REALIZED THEY WERE EXPIRED. HE DID NOT LET THE SURGEON USE THEM. THESE PRODUCT WENT DOWN AS WASTE AND NEVER TOUCHED THE STERILE FIELD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24947848 ↗MalfunctionNov 25, 2025Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT THE CHAMPION SLINGSHOT BROKE. THE BROKEN PIECE WAS RETRIEVED AFTER APPROXIMATELY 15 MINUTES. THERE WERE NO EFFECTS ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23652335 ↗MalfunctionJun 1, 2020Expiration Date Error
IT WAS REPORTED THAT AN EXPIRED PRODUCT WAS USED IN A PROCEDURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10105121 ↗InjuryJul 29, 2019Break
IT WAS REPORTED THAT THE TIP BROKE AND REMAINED INSIDE THE PATIENT.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 8836742 ↗
Other PASSER devices
- NA 7209485Smith & Nephew, Inc. · PASSER202 reports
- FIRSTPASS 22-4038Smith & Nephew, Inc. · PASSER189 reports
- FIRSTPASS 22-4035Smith & Nephew, Inc. · PASSER67 reports
- NanoPass CAT02298Stryker Corporation · PASSER15 reports
- NA 7210752Smith & Nephew, Inc. · PASSER13 reports
- ENDOBUTTON 014396Smith & Nephew, Inc. · PASSER10 reports
- SlingShot CAT02590Stryker Corporation · PASSER8 reports
- NA 014395Smith & Nephew, Inc. · PASSER5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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