Recall archive / FDA device enforcement
Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: ... — FDA record Z-0195-2023
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Sep 14, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL PRODUCTS, REF 220227; MPS Acacia CAT NO: BC-006-04; MEDICAL PRODUCTS SPECIALISTS EXTENSION SET, Catalog Number BC00604, pain control pump accessory
- Reason
- Sterile extension sets were distributed without an expiration date
- Classification
- Class II
- Recalling firm
- Avanos Medical, Inc.
- Quantity
- 1378 units
- Agency-reported status
- Terminated
- Source record identifier
- Z-0195-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | ALL LOT CODES |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: CA, CO, FL, MI, NM, OH, OR, TN, TX, UT, WI
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Nov 16, 2022
- Recall initiation date
- Sep 14, 2022
- Center classification date
- Nov 7, 2022
- Termination date
- Aug 31, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.