Spectra Medical Devices, Llc recalls
Every recall we track for Spectra Medical Devices, Llc — 2 in all, all from 2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Spectra Medical Devices, Llc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 2 | 0 | 0 | 0 | 2 |
What to do if you have a recalled Spectra Medical Devices, Llc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Spectra Medical Devices, Llc recalls
2 shown- Stop using nowMedical device
Spectra Medical Devices, Llc recalls Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule
Spectra Medical Devices recalls 10mL Sodium Chloride Injection ampules due to potential contamination. If sterility is compromised, patients may develop infections, micro-clots, or organ failure. Affected lots include AB3005-AB5008.
Spectra Medical DevicesJul 6, 2026 - Stop using nowDrug
Spectra Medical Devices, Llc recalls Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC,
Spectra Medical Devices recalls Lidocaine HCl Injection ampules due to lack of sterility assurance. Check lot numbers AE4013, AE5032, AE5039, and AE5104.
Spectra Medical DevicesMay 12, 2026
Spectra Medical Devices, Llc recall questions
How many recalls has Spectra Medical Devices, Llc had?
2 recalls from Spectra Medical Devices, Llc are on record with U.S. safety agencies, from 2026 (1 medical device, 1 drug).
What is the most recent Spectra Medical Devices, Llc recall?
Spectra Medical Devices, Llc recalls Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule, dated Jul 6, 2026. Every Spectra Medical Devices, Llc recall is listed on this page, newest first.
What should I do if I have a recalled Spectra Medical Devices, Llc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Spectra Medical Devices, Llc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.