FDA Device recall Z-2109-2021
Stimulen Collagen Moisturizing Lotion, ST9555B
- FDA Device
- Class II
- ongoing
- Published 2021-07-28
On 2021-07-28 the FDA classified a Class II recall of Stimulen Collagen Moisturizing Lotion, ST9555B by Southwest Technologies, citing dose audit failure after sterilization process.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2109-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-05-28 |
| Published | 2021-07-28 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Southwest Technologies |
| Distribution | n/a |
Product
Stimulen Collagen Moisturizing Lotion, ST9555B
Reason
Dose audit failure after sterilization process
Identifiers
| code_info | Lot 2104007, EXP: 02/2024 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Other recalls by Southwest Technologies
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FDA Device · Class II · 2019-12-25 · Southwest Technologies - HYPOTHERMIA MITTS Supportive in Cancer, packaged under the following brands: (a) Elasto-Gel(TM), TM7006 (b) Elasto-Gel(TM), TM7006LV (c) El…
FDA Device · Class II · 2018-05-09 · Southwest Technologies - HYPOTHERMIA CAP Supportive in Cancer, packaged under the following brands: (a) Elasto-Gel(TM), CAP610 (b) Elasto-Gel(TM), CAP610LV (c) Elas…
FDA Device · Class II · 2018-05-09 · Southwest Technologies - HYPOTHERMIA SLIPPERS Supportive in Cancer, packaged under the following brands: (a) Elasto-Gel(TM), SL3000 (b) Elasto-Gel(TM), SL3000LV (c)…
FDA Device · Class II · 2018-05-09 · Southwest Technologies
All Southwest Technologies recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2109-2021%22
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