Inter-Med Llc recalls
Every recall we track for Inter-Med Llc — 8 in all, from 2019–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Inter-Med Llc peaked in 2019 (7); 8 since 2017.
All FDA recall records for Inter-Med 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 | 1 | 6 | 0 | 7 |
| 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) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Inter-Med 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 Inter-Med Llc recalls
2 shown- Lower riskMedical device
Inter-Med Llc recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Inter-Med recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (Catalog 504600-28) due to incorrect package insert that may instruct users to induce vomiting after ingestion, which is unsafe. Affected units contain Ferric Sulfate Gel instructions instead of proper Aluminum Chloride instructions.
Inter-MedMay 27, 2026 - Lower riskMedical device
Inter-Med Llc recalls Vista Dental Products Sodium Hypochlorite - 6%, QTY: 12, 3mL Pre-filled Syringes, REF 502350
Inter-Med recalls 12-count 3mL pre-filled bleach syringes with potential latex-free rubber bung that may degrade over time, causing safety risks.
Inter-MedJun 27, 2019
Inter-Med Llc recall questions
How many recalls has Inter-Med Llc had?
8 recalls from Inter-Med Llc are on record with U.S. safety agencies, from 2019–2026.
What is the most recent Inter-Med Llc recall?
Inter-Med Llc recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28, dated May 27, 2026. Every Inter-Med Llc recall is listed on this page, newest first.
What should I do if I have a recalled Inter-Med 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 Inter-Med 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.