RecallHawk

Scuba Buoyancy Compensator Devices (BCDs) with LP inflator hose

Unknown Manufacturer

Summary

CPSC recalled Scuba Buoyancy Compensator Devices (BCDs) with LP inflator hose by Unknown Manufacturer. Hazard: Defective metal fittings on the inflator hose can cause an airflow restriction and failure to inflate, or improper inflation of the BCD, posing a drowning hazard to the user.. Remedy: Consumers should immediately stop using the recalled scuba BCDs and contact Cressi-sub to receive a free replacement hose with installation instructions including a pre-paid mailing label for returning the recalled hoses. The firm is contacting all known purchasers regarding the recall..

Details

Source

cpsc

External ID

23013

Action Date

2022-10-13

Status

Ongoing

Category

product

Product Description

This recall involves Scuba Buoyancy Compensator Devices (BCDs) with LP inflator hoses. The LP inflator hoses attach to the regulator first stage of the BCD. The following Cressi base models, as identified on the label stitched to the pocket on the BCDs, are included in the recall: Patrol (IC74160), Quartz (JIC74190), Start (IC72170), Start Pro (IC72190), Aquaride (IC74080), Travel Light (IC7406), Commander Evolution (IC771000), and Scorpion (IC77000). Only inflator hoses with serial numbers 007/22, 019/22 or 035/22 stamped into the metal fitting that attaches to the BCDs are included in the recall.

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 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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