Official recall notice
FDA DeviceClass INotable
FDA Recall: Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampule
- Recall date
- 2026-09-16
- Category
- Medical Device
- FDA class
- Class I
Why it was recalled
Hazard
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Product description
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Affected products
UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026), 324586(4/1/2026), 327335(4/1/2026), 329618(9/1/2026), 347199(11/1/2026), 337283(11/1/2026), 350354(11/30/2026), 375449(5/31/2027)