FDA Medical devices recall ·
Phasor Drill recall
- Recall number
- Z-2192-2025
- Date
- (initiated March 21, 2025)
- Company / brand
- Phasor Health, LLC
8944 Kirby Dr, Houston, TX, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 1,064
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Why was it recalled?
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
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: B775270S0, B775320L0, B7754500, B7755300, B7756350. Lot: 241002450, 241002530, 241009450, 241009530, 241016450, 241016530, 241023450, 241023530, 241030450, 241030530, 24112027S, 24121827S, 24122727S, 25012227S, 24082832L, 24102332L, 241227450, 241220635, 250122635, 241227530, 250122530.
Distribution
US: PA, IN, AZ, MO, LA, FL, TX, MA, OH, TN, MI, WV, VA, CA, DE, NH, GA, SC, GU, NY, NJ, MN, WI, NE, WA, IL, AR, PR, VT
States: Arkansas Arizona California Delaware Florida Georgia Illinois Indiana Louisiana Massachusetts Michigan Minnesota Missouri Nebraska New Hampshire New Jersey New York Ohio Pennsylvania Puerto Rico South Carolina Tennessee Texas Virginia Vermont Washington Wisconsin West Virginia
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-2192-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.