Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Pfizer. FDA records under 3 spellings of its name, each linked to the record. See the Pfizer group view.
As of Nov 15, 2026, FDA's public records list Meridian Medical Technologies with 6 510(k) clearances and 3 drug recalls. The most recent is a drug recall dated Mar 12, 2017: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specia….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 12, 2017 | EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical TeClass I · Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medic | Drug recalls |
| Mar 12, 2017 | EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian MedicClass I · Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medic | Drug recalls |
| Jun 6, 2012 | Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count autoinjectors per carton, Rx onlyClass II · Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazep | Drug recalls |
| Jun 11, 2003 | PRIME ECG SYSTEMK030104 · DPS | 510(k) clearances |
| Mar 6, 2002 | PRIME ECG SYSTEMK012414 · DPS | 510(k) clearances |
| Oct 23, 2001 | TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIIIK011058 · DXN | 510(k) clearances |
| May 10, 2001 | BRIDGE III RECEIVERK010794 · DXH | 510(k) clearances |
| Oct 25, 2000 | CARDIOBEEPER CB12/12, MODEL CB12/12K002310 · DXH | 510(k) clearances |
| Mar 17, 1997 | CARDIOBEEPER CB-12LK965101 · DXH | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
