Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported September 2, 2015
Methylcobalamin 5000 mcg/mL Injectable, 2 mL vial, Rx only, Liberty Drug Compound Center, 195 Main St., PO Box 267, Chatham, NJ 07928.
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Liberty Drug & Surgical recalled Methylcobalamin 5000 mcg/mL Injectable, 2 mL vial, Rx only, Liberty Drug Compound Center,… - a moderate-severity action.
Methylcobalamin 5000 mcg/mL Injectable, 2 mL vial, Rx only, Liberty Drug Compound Center,… was recalled by Liberty Drug & Surgical in September 2, 2015. Reason: Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable p…. Check the official notice for the remedy. Verify recall #D-1382-2015 with the FDA Drug before acting.
The recall
Liberty Drug & Surgical issued this moderate-severity FDA Drug recall-Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable p….
- Moderate
- severity level
- Class II
- classification
- September 2, 2015
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1382-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1382-2015) was formally reported on September 2, 2015, with the manufacturer initiating the action on June 15, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Liberty Drug & Surgical is listed as the recalling firm, operating out of Chatham, NJ. Federal records list the affected scope as 5 vials.
The documented reason for this recall is: Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product. Distribution data in the federal record shows the product reached: Physicians, Medical Facilities, and Prescription Specific Patients in NJ and NY. 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
5 vials
Related Recalls
6
5 from same agency
Product description
Methylcobalamin 5000 mcg/mL Injectable, 2 mL vial, Rx only, Liberty Drug Compound Center, 195 Main St., PO Box 267, Chatham, NJ 07928.
Reason for recall
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1382-2015 |
| Date reported | September 2, 2015 |
| Date initiated | June 15, 2015 |
| Recalling firm | Liberty Drug & Surgical |
| Firm location | Chatham, NJ |
| Affected scope | 5 vials |
| Distribution | Physicians, Medical Facilities, and Prescription Specific Patients in NJ and NY |
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-1382-2015) 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? ▼
Methylcobalamin 5000 mcg/mL Injectable, 2 mL vial, Rx only, Liberty Drug Compound Center, 195 Main St., PO Box 267, Chatham, NJ 07928.. Recalled by Liberty Drug & Surgical. Units affected: 5 vials.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Process deficiencies were observed in the sterile ophthalmic and injectable products that could have compromised the sterility of the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 2, 2015. Severity: Moderate. Recall number: D-1382-2015.
Where was the recalled product distributed? ▼
Distribution: Physicians, Medical Facilities, and Prescription Specific Patients in NJ and NY.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1382-2015) 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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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 September 2, 2015. 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.