Stryker Hoffmann II Connecting Rod Micro Recall Issued
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Stryker GmbH is recalling 5,664 units of the Hoffmann II Connecting Rod Micro 3 x 150mm due to potential cracking after cleaning and sterilization.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 13, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-device.
What Happened
Stryker GmbH initiated a voluntary recall of the Hoffmann II Connecting Rod Micro due to potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. The recall is classified as Class II.
Which Products Are Affected
The affected product is Stryker Hoffmann II Connecting Rod Micro 3 x 150mm, Catalog Number: 50796150, GTIN: 04546540389954, all lot numbers. A total of 5,664 units are involved. Distribution includes US nationwide (AL, AZ, CA, CO, FL, GA, ID, IL, KS, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, PA, RI, SC, TN, TX, VA, WI, WV) and the countries of Australia, Austria, Belgium, Canada, Chile, Denmark, France, Germany, Greece, Ireland, Israel, Italy, Japan, Kuwait, Netherlands, Poland, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and UK.
What You Should Do
The recalling firm notified customers via letter. Check inventory for the affected catalog number and lot information.
Why This Matters
This Class II recall addresses a device that may cause temporary or reversible adverse health consequences.
Source
FDA Enforcement Report, recall number Z-2833-2026. https://www.fda.gov
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,199 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 13, 2026.
Frequently Asked Questions
Common questions about this FDA recall.