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Kit: Epidural Pain TQC 20 Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

Official notice

16 Sept 2026

Last checked

22 Sept 2026

CriticalFDA

An official FDA notice concerns Medical Action 306. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2026-09-16. Recall numbers: Z-3106-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

1,960

Recall number

Z-3106-2026

Official notice

2026-09-16

The hazard

Health risk requiring medical assessment

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Other

UDI-DI 10809160367414

Event Ids

99613

Recall Numbers

Z-3106-2026

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · FL

Location 2

US · United States · IA

Location 3

US · United States · KS

Location 4

US · United States · MO

Location 5

US · United States · OH

Location 6

US · United States · VA

Affected area 1

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Medical Action 306. Contact: Medical Action Industries, Inc. 306.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class I

App estimate

critical

Recall details

Recall number

Z-3106-2026

Event id

99613

Units affected

1,960

Status

active

Classification

Class I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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