Spectra Medical Devices, Llc 2026-06-10 Health serious FDA
Health · FDA · Recall #FDA-D-0554-2026
Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by:… Recall
Issued June 10, 2026 · Spectra Medical Devices, Llc
In June 2026, Spectra Medical Devices, Llc recalled the Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by:…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Lack of Assurance of Sterility
What you should do
- 1 Stop using Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Spectra Medical Devices, Llc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Spectra Medical Devices, Llc
- Category
- Health
- Recall date
- June 10, 2026
- Units affected
- Not reported
- Sold at
- USA Nationwide
- Recall number
- FDA-D-0554-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Spectra Medical Devices, Llc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.