Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium C
See all recalls from Medical Action Industries, Inc. 306 →Recalled Product
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Hazard / Issue
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Issued by
FDA
Affected States: IA, VA, MO, KS, FL, OH
Lot/Code Info: 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)
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Kit: Epidural/Pain TQC 20/Cs, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime