Use cautionMedical device recall · FDA · Published March 10, 2022
Wright Medical EasyFuse Instrument Pack Recall: Drill Guide Breakage Risk
Wright Medical recalls EasyFuse Dynamic Compression System Instrument Packs with model FFSP1530 that may jam during surgery, causing drill guide breakage. Affected units have specific lot codes and expiration dates.
“Wright Medical EasyFuse Instrument Pack Recall: Drill Guide Breakage Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/60959-wright-medical-easyfuse-instrument-pack-recall-drill-guide-breakage-risk. Based on FDA recall #Z-0853-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0853-2022%22&limit=1).
Wright Medical Technology, Inc. recalled EasyFuse Dynamic Compression System Instrument Packs due to a jamming hazard that can cause the drill guide to break, according to the FDA on March 10, 2022.
How to tell if you have it
Brand: Wright Medical
Product: EasyFuse Dynamic Compression System Instrument Pack
Model Number: FFSP1530
UDI: 00889797103565
Lot Codes: 781853-110321 (Expiration Date: 11/03/2029) and 780395-112221 (Expiration Date: 12/03/2029)
Distribution: US distribution to Florida, North Carolina, Ohio, and Texas
Quantity: 176 packs
The hazard
The drill and adjustable drill guide can jam or bind intraoperatively, resulting in the drill guide breaking, according to the FDA.
Context
GovInfoNow's records show Wright Medical Technology, Inc. has 20 other recalls on record since March 14, 2018. Other recent recalls of similar products include Charlotte Claw Screw Recall (August 18, 2026), Stryker Infinity Resection Adjustment Block Recall (March 6, 2024), and Stryker Infinity Alignment Frame Distal Sub-Assembly Recall (June 13, 2023).
How to tell if you have this one
Check for model number FFSP1530 on the instrument pack. Affected units have lot codes 781853 (expires 11/03/2029) or 780395 (expires 12/03/2029).
Brand
Wright Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Model Number
Look for model number FFSP1530 on the instrument pack to confirm if it is affected.
Contact Manufacturer
Contact Wright Medical Technology, Inc. for further assistance with the recall.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “US distribution to Florida, North Carolina, Ohio, and Texas” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, North Carolina, Ohio, Texas.
Recall timeline
FDA terminated this recall 4.1 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0853-2022 (March 10, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0853-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.