ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister pack with Tyvek lid. T...
FDA Device Recall #Z-1530-2013 — Class II — May 13, 2013
Recall Summary
| Recall Number | Z-1530-2013 |
| Classification | Class II — Moderate risk |
| Date Initiated | May 13, 2013 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Ethicon Endo-Surgery Inc |
| Location | Cincinnati, OH |
| Product Type | Devices |
| Quantity | 57,540 Units |
Product Description
ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister pack with Tyvek lid. The ECHELON and ECHELON FLEX families of Endoscopic Linear Cutters (articulating and straight) are sterile, single patient use instruments that simultaneously cut and staple tissue. There are six staggered rows of staples, three on either side of the cut line. The ECHELON 60 instruments have a staple line that is approximately 60 mm long and a cut line that is approximately 57 mm long. The shaft can rotate freely in both directions and an articulation mechanism on articulating instruments enables bending the distal portion of the shaft to facilitate lateral access of the operative site. The instruments are shipped without a reload and must be loaded prior to use. A staple retaining cap on the reload protects the staple leg points during shipping and transportation. The instruments'¿" lock-out feature is designed to prevent a used reload from being refired.
Reason for Recall
Ethicon Endo-Surgery is initiating a voluntary worldwide recall for ECHELON 60mm Black Reload (ECR60T) due to the potential for incomplete staple line formation from reload damage during the firing sequence.
Distribution Pattern
Worldwide Distribution - US Nationwide all fifty states and including the countries of Canada, Belgium, India, Malaysia, Saudi Arabia, Brazil, Israel, Mexico, Singapore, Jordan, New Zealand, Taiwan, Chile, Korea, Puerto Rico, Turkey, Columbia, Kuwait, Qatar, United Arab Emirates, Egypt, Lebanon and Russia.
Lot / Code Information
The following lot numbers and associated expiration dates are affected by this recall: J4AY8Z 5/15/2013, J4C00J 6/15/2013, J4C87R 7/15/2013, J4CC1F 8/15/2013, J4CD2X 8/15/2013, J4CF3D 9/15/2013, J4CJ0E 9/15/2013, J4CJ78 9/15/2013, J4CK2P 9/15/2013, J4CM9X 10/15/2013, J4CR2H 10/15/2013, J4CT5H 11/15/2013, J4CU86 11/15/2013, J4CV1W 11/15/2013, J4CV5H 11/15/2013, K4C149 12/15/2013, K4C17W 12/15/2013, K4C33U 12/15/2013, K4C41C 12/15/2013, K4C600 1/15/2014, K4C64A 1/15/2014, 4C728 1/15/2014, K4C82K 1/15/2014, K4C88F 1/15/2014, K4C94W 1/15/2014, K4CC0L 2/15/2014, CC8L 2/15/2014, K4CD1E 2/15/2014, K4CF1P 2/15/2014, K4CF5D 2/15/2014, K4CG18 3/15/2014, K4CG4J 3/15/2014, K4CG8P 3/15/2014, K4CH44 3/15/2014, K4CK0W 3/15/2014,
Other Recalls from Ethicon Endo-Surgery Inc
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0147-2026 | Class II | ECHELON LINEAR Cutters Reload 80 mm Blue, inten... | Sep 11, 2025 |
| Z-1746-2025 | Class I | Endopath Echelon Vascular White Reload for Adva... | Apr 22, 2025 |
| Z-0834-2024 | Class II | ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SUR... | Dec 11, 2023 |
| Z-2355-2021 | Class II | HARMONIC HD 1000i Shears (20cm Shaft Length)-in... | Jul 20, 2021 |
| Z-2356-2021 | Class II | HARMONICHD 1000i Shears (36cm Shaft Length)-ind... | Jul 20, 2021 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.