Notice names this product. GRI Medical & Electronic Technology Co’s HALYARD Laparoscopy Comprehensive Pack II REF is named in FDA Class II recall Z-0077-2027. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter Identifying details: UDI-DI: 10680651493320 (unit level), 30680651493324 (case level) Lot Numbers: GL25271CXA-Expiry Date: 2029/3/30; GL25296CXA-Expiry Date: 2029/3/30; GL26076CXA-Expiry Date: 2029/5/31. Units affected: 396 kits. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
Company / brand: GRI Medical & Electronic Technology Co recalls
Affected product: HALYARD Laparoscopy Comprehensive Pack II REF recall status
Official ID Z-0077-2027 · Official record ↗
See all GRI Medical & Electronic Technology Co recalls →
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.