Kit: Single Shot Epidural 20/Cs, REF: 59553
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
- Agency
- FDA Device
- Recall date
- Jul 23, 2026
- Status
- Ongoing
- Company
- Medical Action Industries, Inc. 306
1. What product was recalled?
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Quantity: 1,960
Code or lot text: 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)
- LOT
- 324586(4/1/2026)
- LOT
- 327335(4/1/2026)
- LOT
- 329618(9/1/2026)
- LOT
- 337283(11/1/2026)
- LOT
- 347199(11/1/2026)
- LOT
- 350354(11/30/2026)
- LOT
- 375449(5/31/2027)
- LOT
- UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026)
- RECALL-NUMBER
- Z-3106-2026
Kit: Single Shot Epidural 20/Cs, REF: 59553
Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Quantity: 3,606
Code or lot text: REF/UDI-DI/Lot(Expiration Date): 59553/10809160010518/330274(9/1/2026), 331036(11/1/2026), 332995(11/1/2026), 333957(11/1/2026), 338894(11/1/2026); 83945B/10809160444269/330827(10/10/2026), 330907(10/10/2026), 333956(11/1/2026), 350340(11/1/2026), 351266(11/30/2026), 373674(5/31/2027)
- LOT
- 330907(10/10/2026)
- LOT
- 331036(11/1/2026)
- LOT
- 332995(11/1/2026)
- LOT
- 333956(11/1/2026)
- LOT
- 333957(11/1/2026)
- LOT
- 338894(11/1/2026)
- LOT
- 350340(11/1/2026)
- LOT
- 351266(11/30/2026)
- LOT
- 373674(5/31/2027)
- LOT
- 83945B/10809160444269/330827(10/10/2026)
- LOT
- REF/UDI-DI/Lot(Expiration Date): 59553/10809160010518/330274(9/1/2026)
- RECALL-NUMBER
- Z-3107-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Florida, Iowa, Kansas, Missouri, Ohio, Virginia
View source evidence for state distribution
- Florida: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Iowa: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Kansas: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Missouri: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Ohio: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Virginia: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Device source
The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.