PlainRecalls

CPSC, Cressi-Sub Announce Recall of SCUBA Buoyancy Compensators

Reported: February 23, 2005 Initiated: February 23, 2005 #05121 About 1,000 units

Cressi-sub S.p.A., of Genoa, Italy issued this CPSC recall on February 23, 2005. Classified as Moderate severity. Approximately About 1,000 units are affected. The recall was issued because: A slow leak from the shoulder exhaust caused by expansion of an internal cable housing could result in slow deflation. …. 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 #05121) was formally reported on February 23, 2005. It is classified under Moderate severity, with a current status of Active. Cressi-sub S.p.A., of Genoa, Italy is listed as the recalling firm. Federal records indicate About 1,000 units are affected.

The documented reason for this recall is: A slow leak from the shoulder exhaust caused by expansion of an internal cable housing could result in slow deflation. This could impact the diver's ability to control buoyancy. 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: Customers can return the product to a Cressi-sub-authorized dive shop to have the product retro-fitted with a free replacement internal cable housing. Buoyancy Compensator devices with a black retain… — 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. 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 21 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 1,000

Related Recalls

6

0 from same agency

Product Description

Buoyancy Compensator devices provide buoyancy control for scuba divers by allowing them to inflate or deflate the devices. The recalled buoyancy compensators have model numbers J107, J113, J115, and J119. The numbers appear on the top right-hand corner of the unit (on the shoulder). "CRESSI" is written on the buoyancy control devices.

Reason for Recall

A slow leak from the shoulder exhaust caused by expansion of an internal cable housing could result in slow deflation. This could impact the diver's ability to control buoyancy.

Remedy

Customers can return the product to a Cressi-sub-authorized dive shop to have the product retro-fitted with a free replacement internal cable housing. Buoyancy Compensator devices with a black retaining ring around the yellow inflate button on the inflation mechanism, and an adjoining gray cover assembly (bypass case), which screws onto the inflator, are subject to this recall and must be retro-fitted. Devices which have yellow retaining rings and black cover assemblies have been retro-fitted.

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 05121
Date reported February 23, 2005
Date initiated February 23, 2005
Recalling firm Cressi-sub S.p.A., of Genoa, Italy
Units affected About 1,000
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 1,000 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?
Buoyancy Compensator devices provide buoyancy control for scuba divers by allowing them to inflate or deflate the devices. The recalled buoyancy compensators have model numbers J107, J113, J115, and J119. The numbers appear on the top right-hand corner of the unit (on the shoulder). "CRESSI" is written on the buoyancy control devices.. Recalled by Cressi-sub S.p.A., of Genoa, Italy. Units affected: About 1,000.
Why was this product recalled?
A slow leak from the shoulder exhaust caused by expansion of an internal cable housing could result in slow deflation. This could impact the diver's ability to control buoyancy.
What should consumers do?
Customers can return the product to a Cressi-sub-authorized dive shop to have the product retro-fitted with a free replacement internal cable housing. Buoyancy Compensator devices with a black retaining ring around the yellow inflate button on the inflation mechanism, and an adjoining gray cover assembly (bypass case), which screws onto the inflator, are subject to this recall and must be retro-fitted. Devices which have yellow retaining rings and black cover assemblies have been retro-fitted.
Which agency issued this recall?
This recall was issued by the CPSC on February 23, 2005. Severity: Moderate. Recall number: 05121.
How do I check if my product is affected by a recall?
Check the product description and recall number (05121) 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.

Nearby Recalls in This Category

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

Compare this recall with Endo-Model Replacement Plateau; Item Number: 15-0027/11; →

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).