FDA Enforcement
Class II
Ongoing
BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Recall: Z-2182-2026
·
Reported May 20, 2026
Enforcement
- Recall Number
- Z-2182-2026
- Event ID
- 98708
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Stryker Sustainability Solutions
- Voluntary / Mandated
- Voluntary: Firm initiated
- Report Date
- May 20, 2026
- Initiation Date
- April 10, 2026
- Classification Date
- May 13, 2026
- Address
- 1810 W Drake Dr, Tempe, AZ, 85283-4327, United States
Description
BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Reason
Incomplete seals on sterile product
Code Info
UDI 00885825003739, Lot Numbers 4573219, 4869696, 4992244, 4999900, 5025367, 5038410, 5085389, 4804556, 4971805, 4992245, 4999902, 5032111, 5043783, 4804558, 4971806, 4992246, 5012684, 5032112, 5043784, 4809474, 4990763, 4992247, 5012708, 5032113, 5043785, 4829451, 4990764, 4993772, 5012709, 5033926, 5043787, 4835199, 4990769, 4997966, 5012711, 5033927, 5056579, 4841812, 4992243, 4998135, 5012726, 5033928, 5056828.
Distribution
US Nationwide and the countries of Israel and Canada.
Quantity
44 units