REMINGTON MEDICAL, INC.
4 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (4)
Registered facilities (3)
- REMINGTON MEDICAL, INC. FEI 1000132370 · GA
- Remington Medical, S.A. FEI 3009265194 · DO
- Remington Medical, Inc. FEI 3007014520 · GA
Recalls & enforcement
- Class IIOngoing2023-11-03There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
- Class IITerminated2022-12-02The stylet is longer than specified on the label
- Class IITerminated2014-03-05Remington Medical discovered an error on the FL-601-97 IFU; part number IFU-RM-0154. Specifically, the polarity for the black chuck in the picture is wrong. It shows (+), but should show (-).
- Class IITerminated2012-08-29Sterility of the product may be compromised.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “REMINGTON MEDICAL, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9006473-remington-medical-inc/
Alerts for REMINGTON MEDICAL, INC.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.