Severity
Critical
CriticalClass IOngoing
FDA Drug recall · Reported May 10, 2017
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Meridian Medical Technologies a Pfizer Company recalled EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Sp… - a critical-severity action.
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Sp… was recalled by Meridian Medical Technologies a Pfizer Company in May 10, 2017. Reason: Defective Delivery System; reports of the device failing to activate which could result in a patient not rece…. Check the official notice for the remedy. Verify recall #D-0691-2017 with the FDA Drug before acting.
The recall
Meridian Medical Technologies a Pfizer Company issued this critical-severity FDA Drug recall-Defective Delivery System; reports of the device failing to activate which could result in a patient not rece….
- Critical
- severity level
- Class I
- classification
- May 10, 2017
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0691-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0691-2017) was formally reported on May 10, 2017, with the manufacturer initiating the action on March 12, 2017. It is classified under Critical severity (Class I), with a current status of Ongoing. Meridian Medical Technologies a Pfizer Company is listed as the recalling firm, operating out of Brentwood, MO. Federal records list the affected scope as 92,544 2-pak (U.S.); 198,579 syringes (O.U.S.).
The documented reason for this recall is: Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication Distribution data in the federal record shows the product reached: Nationwide and Puerto Rico, Argentina, Austria, Australia, Belgium, Chile, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Ireland, Italy, Japan, Latvia, Lithuania, Netherlands, New Zealand, Norway,…. 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
92,544 2-pak (U.S.); 198,579 syringes (O.U.S.)
Related Recalls
6
5 from same agency
Product description
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Reason for recall
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | D-0691-2017 |
| Date reported | May 10, 2017 |
| Date initiated | March 12, 2017 |
| Recalling firm | Meridian Medical Technologies a Pfizer Company |
| Firm location | Brentwood, MO |
| Affected scope | 92,544 2-pak (U.S.); 198,579 syringes (O.U.S.) |
| Distribution | Nationwide and Puerto Rico, Argentina, Austria, Australia, Belgium, Chile, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Ireland, Italy, Japan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Poland, Portugal, R… |
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-0691-2017) 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.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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? ▼
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.. Recalled by Meridian Medical Technologies a Pfizer Company. Units affected: 92,544 2-pak (U.S.); 198,579 syringes (O.U.S.).
Why was this product recalled? ▼
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 10, 2017. Severity: Critical. Recall number: D-0691-2017.
Where was the recalled product distributed? ▼
Distribution: Nationwide and Puerto Rico, Argentina, Austria, Australia, Belgium, Chile, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Ireland, Italy, Japan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Poland, Portugal, Romania, Saudi Arabia, Singapore, Slovakia, Slovenia, Sweden, Switzerland, Taiwan, Thailand, United Kingdom. There has been no U.S. government or military distribution..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0691-2017) 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 May 10, 2017. 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.