Teva Epinephrine Auto-Injector Recall: Out-of-specification trigger force
Teva recalls Epinephrine Injection USP 0.3 mg auto-injectors due to out-of-specification trigger force in a non-marketed lot. This may affect safety during use.
Lower-risk recall
CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.
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What happened, in plain English
Teva is recalling a specific lot of epinephrine auto-injectors because the trigger force was out of specification. This could potentially affect the device's safety during use, though the recall is limited to a specific non-marketed lot. Read more at govinfonow.com/recall/37346-teva-epinephrine-auto-injector-recall-out-of-specification-trigger-force.
Source Summary by GovInfoNow · govinfonow.com/recall/37346-teva-epinephrine-auto-injector-recall-out-of-specification-trigger-force · Updated October 5, 2026 · FDA enforcement record: FDA #D-1260-2020
Cite this page
“Teva Epinephrine Auto-Injector Recall: Out-of-specification trigger force.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37346-teva-epinephrine-auto-injector-recall-out-of-specification-trigger-force. Based on FDA recall #D-1260-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1260-2020%22&limit=1).
Why it’s dangerous
The recall involves a non-marketed lot where the trigger force for the epinephrine injector was out of specification. This could mean the device might not function properly during an emergency, though the risk is limited to this specific lot.
Who’s affected
People with a prescription for Teva's Epinephrine Injection USP 0.3 mg auto-injector who received the specific lot number 007F19AA (expiring April 2021) are affected. Those using the device for medical emergencies are at most risk.
How to tell if you have this one
Check the product label for the lot number 007F19AA and expiration date of April 2021. The product is a prescription-only epinephrine auto-injector with NDC code 0093-5986-27.
- Brand
Teva- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number 007F19AA and expiration date of April 2021 on the product label.
How this recall unfolded
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1260-2020 (March 5, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1260-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.