Amazon.com from September 2021 through February 2023 for between $170 and $400. recalls
2 recalls recorded since 2018, most recently on 22 February 2024. Status and classification are as published by the CPSC.
Recalls2
Ongoing (FDA)0
Terminated or completed0
Class I (FDA)0
Announced Consumer products
- Recall started
- 22 February 2024
- Reason
- The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
- Remedy
- Consumers should immediately stop using the biometric feature of the recalled safe, remove the batteries from the safe, and only use the key when storing firearms. Contact BBRKIN to receive a repair kit or to receive a free replacement safe. Consumers will be asked to disable the biometric reader and email a photo of the disabled biometric reader to support@bbrkin.com in order to receive a replacement safe. The instructions on how to safely disable the biometric reader are also located at www.securitysafe.store/recallreplacement.
- Recall number
- 24128
- MouTec brand Biometric Firearm Safes
CPSC recall notice
Announced Consumer products
- Recall started
- 22 February 2024
- Reason
- The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death if the safe is used to store firearms.
- Remedy
- Consumers should immediately stop using the biometric lock feature, remove the batteries, and only use the key for the recalled safes to store their items until they get the free replacement. Contact Machir to receive instructions on disabling the biometric lock feature and on how to receive a free replacement safe. Consumers will be asked to disable the biometric reader and email a photo of the disabled biometric reader to Info@machir.com in order to receive a replacement safe. The instructions on how to safely destroy the biometric reader are also located at http://machir.com/biorecall/.
- Recall number
- 24129
- Machir Biometric Personal Safes
CPSC recall notice
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.