1st stage scuba regulators
Summary
CPSC recall: 1st stage scuba regulators. By XDEEP, of Poland. Hazard: A defective screw on the turret connection can break, posing a risk of severe injury and drowning hazard for divers.. Remedy: Consumers should immediately stop using the recalled scuba regulators and contact XDEEP for a full refund or free replacement. The replacement includes a different model. Consumers can return the recalled regulator to the place of purchase or contact Tec Dive Gear to obtain a parcel label to return the
Details
Source
CPSC Consumer Product Recall
External ID
9540
Action Date
2023-02-23
Status
Recalled
Category
consumer_product
Product Description
This recall involves 1st stage scuba regulators with model number NX700. The model number is inscribed on one side of th
Company
Context & Analysis
This is a unclassified recall.
This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
XDEEP, of Poland has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (XDEEP, of Poland) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does XDEEP, of Poland have FDA actions?
XDEEP, of Poland has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9540" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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