HOFFMANN 5079-6-030Recalls & reported problems
Stryker GmbH · Connecting Rod Micro · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 04546540389893), received between Aug 24, 2026 and Aug 26, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Crack” (5 reports).
1 FDA recall record name this device's identifier, 1 still open.
6 other recalls cover devices cleared under the same FDA submission (K033476); 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.
Reports received per month
Recalls naming this device
- Jul 1, 2026Open, Classified
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Z-2827-2026 · Root cause: Device Design · FDA record ↗
Most reported problems
Device problems
- Crack5
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 26, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50456686 ↗MalfunctionAug 24, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50418745 ↗MalfunctionAug 24, 2026Crack
Cracks identified in Hoffmann Micro carbon rods.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50418732 ↗MalfunctionAug 24, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50418716 ↗MalfunctionAug 24, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50410154 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K033476. One submission often covers many models, so check the product and lot details in each record.
- Z-2829-2026 · Jul 1, 2026 · Open, ClassifiedStryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.
- Z-2831-2026 · Jul 1, 2026 · Open, ClassifiedStryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.
- Z-2832-2026 · Jul 1, 2026 · Open, ClassifiedStryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120.
- Z-2828-2026 · Jul 1, 2026 · Open, ClassifiedStryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.
- Z-2830-2026 · Jul 1, 2026 · Open, ClassifiedStryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.
- Z-2833-2026 · Jul 1, 2026 · Open, ClassifiedStryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.