Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported July 3, 2013
0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7132-02
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Hospira Inc. recalled 0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL … - a moderate-severity action.
0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL … was recalled by Hospira Inc. in July 3, 2013. Reason: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking ba…. Check the official notice for the remedy. Verify recall #D-613-2013 with the FDA Drug before acting.
The recall
Hospira Inc. issued this moderate-severity FDA Drug recall-Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking ba….
- Moderate
- severity level
- 137K units
- affected scope
- Class II
- classification
- July 3, 2013
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-613-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-613-2013) was formally reported on July 3, 2013, with the manufacturer initiating the action on May 4, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Hospira Inc. is listed as the recalling firm, operating out of Lake Forest, IL. Federal records list the affected scope as 136,584 units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags. Distribution data in the federal record shows the product reached: Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia. Distribution scope 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, 5 from FDA Drug - 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
136,584 units
Related Recalls
6
5 from same agency
Product description
0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7132-02
Reason for recall
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-613-2013 |
| Date reported | July 3, 2013 |
| Date initiated | May 4, 2012 |
| Recalling firm | Hospira Inc. |
| Firm location | Lake Forest, IL |
| Affected scope | 136,584 units |
| Distribution | Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia |
Profile values are sourced directly from the official FDA Drug 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 (D-613-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug 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 Drug 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? ▼
0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7132-02. Recalled by Hospira Inc.. Units affected: 136,584 units.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 3, 2013. Severity: Moderate. Recall number: D-613-2013.
Where was the recalled product distributed? ▼
Distribution: Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-613-2013) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported July 3, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.