Severity
Moderate
SI Tech, of Sweden issued this CPSC recall on April 14, 2022. Classified as Moderate severity. Approximately About 1,670 (In addition, about 28 were sold in Canada) units are affected. The recall was issued because: The internal part in the valve can malfunction while in use, causing loss of inflation and thermal protection, posing a…. 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.
This CPSC action (record #22115) was formally reported on April 14, 2022. It is classified under Moderate severity, with a current status of Active. SI Tech, of Sweden is listed as the recalling firm. Federal records indicate About 1,670 (In addition, about 28 were sold in Canada) units are affected, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: The internal part in the valve can malfunction while in use, causing loss of inflation and thermal protection, posing a risk of hypothermia to the consumer. 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 should immediately stop using the dry suits with the recalled inflation valve and contact Ocean Equipment to receive a notification form and shipping information to return the recalled valv… — 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 6 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 4 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.
Severity
Moderate
Units Affected
About 1,670 (In addition, about 28 were sold in Canada)
Related Recalls
6
6 from same agency
This recall involves the Shell Inflation Valves with Int'l Nipples that come with diving dry suits and are also sold separately. The Shell Inflation Valve is used in recreational and technical diving. The recalled valve inflates the diving dry suit to allow the diver to equalize air pressure while descending in the water by pressing on the valve and it provides thermal protection to the diver. The model number and batch code are stamped on the inside of the recalled valve. Instructions on how to find and identify the batch code can be found at www.sitech.se. Model Number 25210 JD1, JE2, JE5, JE6, JF6, JG2, JK6, JK9, JKA, JL1, JL3, KA7, KB8, KG2, KH3, KH4, KK7, KL3, LC1, LC2, LC4, LC7, LC9, LD2, LD6, LD7, LD8 25215 JG1, KA9, LC5
The internal part in the valve can malfunction while in use, causing loss of inflation and thermal protection, posing a risk of hypothermia to the consumer.
Consumers should immediately stop using the dry suits with the recalled inflation valve and contact Ocean Equipment to receive a notification form and shipping information to return the recalled valve free of charge. The valve part will be replaced by trained technicians who are exclusively authorized to update the valve with a free replacement valve part.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 22115 |
| Date reported | April 14, 2022 |
| Date initiated | April 14, 2022 |
| Recalling firm | SI Tech, of Sweden |
| Units affected | About 1,670 (In addition, about 28 were sold in Canada) |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
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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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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
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.
Read our methodology — how this data is sourced, computed, and verified.
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).