Southmedic, Inc. recalls
Every recall we track for Southmedic, Inc. — 4 in all, from 2017–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Southmedic, 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 | 2 | 0 | 2 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Southmedic, 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 Southmedic, Inc. recalls
4 shown- Lower riskMedical device
Southmedic, Inc. recalls Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO
Southmedic recalls safety cartridges with lot W92761 sold as sterile but were not properly sterilized. Consumers should check product labels for the lot number and contact Southmedic for details.
SouthmedicOct 27, 2022 - Use cautionMedical device
Southmedic, Inc. recalls OxyMask O2 Adult REF OM-1125-14
Southmedic recalls OxyMask O2 Adult REF OM-1125-14 due to risk of oxygen tubing disconnecting, causing inadequate oxygen delivery to patients.
SouthmedicMay 25, 2021 - Lower riskMedical device
Southmedic, Inc. recalls Southmedic Sterile Disposable Scalpel Rx only Scalpels are intended to be used in various medical procedures for
Southmedic recalls sterile disposable scalpels due to non-sterile products in some lots. This could lead to infection during medical procedures. Affected lots include 092517.
SouthmedicNov 6, 2017 - Lower riskMedical device
Southmedic, Inc. recalls Southmedic Oxygen Masks with EtCO2 sampling line part number OM-2125-8, 25 masks per case. Minimal contact, open oxygen
Southmedic recalls oxygen masks with EtCO2 sampling line (part number OM-2125-8) due to potential loose or missing CO2 diffusers causing non-functioning. Affected units include specific model numbers and lot codes.
SouthmedicOct 17, 2017
Southmedic, Inc. recall questions
How many recalls has Southmedic, Inc. had?
4 recalls from Southmedic, Inc. are on record with U.S. safety agencies, from 2017–2022.
What is the most recent Southmedic, Inc. recall?
Southmedic, Inc. recalls Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO, dated Oct 27, 2022. Every Southmedic, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Southmedic, 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 Southmedic, 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.