RecallHawk

Blitz and Blitz 777 air rifles

Unknown Manufacturer

Summary

CPSC recalled Blitz and Blitz 777 air rifles by Unknown Manufacturer. Hazard: The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from projectile hazard.. Remedy: Consumers should stop using the recalled air rifles immediately, make sure they are unloaded and contact HatsanUSA for a free trigger assembly replacement which will be mailed along with instructions. If the consumer does not want to complete the replacement of the air rifle trigger assembly on their own, HatsanUSA will provide a prepaid package to ship the product to HatsanUSA for inspection and replacement..

Details

Source

cpsc

External ID

27025

Action Date

2026-10-15

Status

Ongoing

Category

product

Product Code

Air Rifles/Air Guns/BB Guns & Accessories

Product Description

This recall involves all units of the Hatsan Blitz and Blitz 777 pellet shooting air rifles sold from February 2020 through March 2026. Both the Blitz and Blitz 777 pellet air rifles were sold in .22, .25 and .30 calibers. The pellet air rifles are gas operated and select-fire (semi-auto/full-auto) pre-charged pneumatic (PCP). They are black and feature a synthetic stock, a carbon fiber air tank mounted beneath the barrel and a rotary magazine feed. Serial numbers and manufacturing dates are engraved on the right side of the receiver above the bolt. On the left side of the receiver is the Hatsan logo, featuring a circular mark, with the word “HATSAN” next to a graphic of a bow and arrow. The model name “BLITZ” or “BLITZ 777” is also marked on the left side of the receiver.

Context & Analysis

Unknown Manufacturer has 1455 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1455 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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