PlainRecalls

Silent Diving Systems Recalls Scuba Diving Hoses Due to Drowning Hazard

Reported: February 24, 2009 Initiated: February 24, 2009 #09722 About 820 units

Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom issued this CPSC recall on February 24, 2009. Classified as Moderate severity. Approximately About 820 units are affected. The recall was issued because: Diving hoses may have been made without crimps, which can allow gas to leak or water to enter into the re-breather unit…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This CPSC action (record #09722) was formally reported on February 24, 2009. It is classified under Moderate severity, with a current status of Active. Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom is listed as the recalling firm. Federal records indicate About 820 units are affected.

The documented reason for this recall is: Diving hoses may have been made without crimps, which can allow gas to leak or water to enter into the re-breather unit of the scuba diving equipment, posing a drowning hazard to the user. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers with the recalled hoses should immediately stop using the hoses and contact Silent Diving Systems to receive a replacement hose. All known purchasers have been contacted directly by Silent … — consumers holding this product should act on that instruction rather than relying on general guidance.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 1 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 17 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

About 820

Related Recalls

6

1 from same agency

Product Description

The crimped hoses are used to carry the air supply in the re-breathing diving system. The hoses were sold on three re-breathing models: Inspiration, Evolution and Evolution Plus. Hoses with a smooth (uncrimped) collar and with the model numbers listed below are included in the recall: AP300/15 ADV Supply Hose RB20/03 Oxygen Injection Hose EV20/03 Oxygen Injection Hose RB20/10 Buzzer Hose EV11A/1 Vision Handset Hose RB11A/1 Classic Handset Hose RB11/B Handset Hose AP300/10 ADV Hose AP300/38 ADV Hose Hoses with eight flats on the hose collar have been crimped and are not included in the recall.

Reason for Recall

Diving hoses may have been made without crimps, which can allow gas to leak or water to enter into the re-breather unit of the scuba diving equipment, posing a drowning hazard to the user.

Remedy

Consumers with the recalled hoses should immediately stop using the hoses and contact Silent Diving Systems to receive a replacement hose. All known purchasers have been contacted directly by Silent Diving Systems regarding the recall.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 09722
Date reported February 24, 2009
Date initiated February 24, 2009
Recalling firm Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom
Units affected About 820
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 820 units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
The crimped hoses are used to carry the air supply in the re-breathing diving system. The hoses were sold on three re-breathing models: Inspiration, Evolution and Evolution Plus. Hoses with a smooth (uncrimped) collar and with the model numbers listed below are included in the recall: AP300/15 ADV Supply Hose RB20/03 Oxygen Injection Hose EV20/03 Oxygen Injection Hose RB20/10 Buzzer Hose EV11A/1 Vision Handset Hose RB11A/1 Classic Handset Hose RB11/B Handset Hose AP300/10 ADV Hose AP300/38 ADV Hose Hoses with eight flats on the hose collar have been crimped and are not included in the recall.. Recalled by Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom. Units affected: About 820.
Why was this product recalled?
Diving hoses may have been made without crimps, which can allow gas to leak or water to enter into the re-breather unit of the scuba diving equipment, posing a drowning hazard to the user.
What should consumers do?
Consumers with the recalled hoses should immediately stop using the hoses and contact Silent Diving Systems to receive a replacement hose. All known purchasers have been contacted directly by Silent Diving Systems regarding the recall.
Which agency issued this recall?
This recall was issued by the CPSC on February 24, 2009. Severity: Moderate. Recall number: 09722.
How do I check if my product is affected by a recall?
Check the product description and recall number (09722) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

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Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).