T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe.

Incorrect labeling of the expiration date

Recall #: Z-1808-2015
Affected scope: 1,080 units (3 cases)
Initiated: February 9, 2015

Compiled from official public sources by the publisher. · Updated September 2026

Mrp, LLC dba Amusa recalled T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 … - a moderate-severity action.

T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 … was recalled by Mrp, LLC dba Amusa in June 24, 2015. Reason: Incorrect labeling of the expiration date. Check the official notice for the remedy. Verify recall #Z-1808-2015 with the FDA Devices before acting.

The recall

Mrp, LLC dba Amusa issued this moderate-severity FDA Devices recall-Incorrect labeling of the expiration date.

Moderate
severity level: Class II
classification: June 24, 2015
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-1808-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe.

Reason for recall

Incorrect labeling of the expiration date

Recall Profile

Structured summary of the FDA Devices recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	Z-1808-2015
Date reported	June 24, 2015
Date initiated	February 9, 2015
Recalling firm	Mrp, LLC dba Amusa
Firm location	Nashville, TN
Affected scope	1,080 units (3 cases)
Distribution	US distribution to CA only.

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (Z-1808-2015) and product description against the item you own. Search the archive
Confirm the current status with FDA Devices before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe.. Recalled by Mrp, LLC dba Amusa. Units affected: 1,080 units (3 cases).

Why was this product recalled? ▼

Incorrect labeling of the expiration date

Which agency issued this recall? ▼

This recall was issued by the FDA Devices on June 24, 2015. Severity: Moderate. Recall number: Z-1808-2015.

Where was the recalled product distributed? ▼

Distribution: US distribution to CA only..

Should I stop using a recalled medication or medical device? ▼

Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

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Similar severity · nearest report date

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This recall: FDA Devices, reported June 24, 2015. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026