FDA Medical devices recall ·
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing recall
- Recall number
- Z-0038-2025
- Date
- (initiated August 14, 2024)
- Company / brand
- 3M Company
3m Center 2510 Conway Ave, Saint Paul, MN, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 10,000 units
- Hazard tags
- Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R
Why was it recalled?
Contamination with foreign substance matter
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI/DI 10707387802223 (carton), UDI/DI 30707387802227 (each), Lot Number 33WWRRR
Distribution
International distribution to the country of South Korea.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0038-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.