AMD Medicom Inc. recalls
Every recall we track for AMD Medicom Inc. — 7 in all, from 2019–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from AMD Medicom Inc. peaked in 2023 (3); 7 since 2017.
All FDA recall records for AMD Medicom Inc. 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 | 2 | 0 | 2 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 3 | 0 | 3 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 2 | 0 | 0 | 2 |
What to do if you have a recalled AMD Medicom Inc. 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 AMD Medicom Inc. recalls
3 shown- Use cautionMedical device
AMD Medicom Inc. recalls Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,
AMD Medicom recalls Ritmed Neurological Sponges (0.5x0.5in to 1.0x3.0in) due to potential endotoxin levels that could cause neurovascular issues during surgery. Affected lots distributed after May 2022.
AMD MedicomMay 8, 2026 - Lower riskMedical device
AMD Medicom Inc. recalls PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)
AMD Medicom Inc. recalls anti-fog earloop masks (item code 127-757: blue, ASTM Level 3) made on unvalidated equipment. These masks may not meet safety standards.
PATTERSON PROCEDUREDec 21, 2023 - Lower riskMedical device
AMD Medicom Inc. recalls MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040
Medicom recalls Level :2 masks (Item 2040) that may be in Level 3 boxes. Using these masks risks lower protection than intended. Affected masks were sold with Lot 1917.
MedicomOct 11, 2019
AMD Medicom Inc. recall questions
How many recalls has AMD Medicom Inc. had?
7 recalls from AMD Medicom Inc. are on record with U.S. safety agencies, from 2019–2026.
What is the most recent AMD Medicom Inc. recall?
AMD Medicom Inc. recalls Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,, dated May 8, 2026. Every AMD Medicom Inc. recall is listed on this page, newest first.
What should I do if I have a recalled AMD Medicom Inc. 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 AMD Medicom Inc. 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.