PlainRecalls
CPSC Moderate Active

Johnson Outdoors Diving Recalls Dive Computers Due to Injury Hazard

Reported: August 5, 2014 Initiated: August 5, 2014 #14249

Product Description

This recall involves the Aladin2 wrist dive computer that monitors depth, dive time, decompression status and temperature. The computer is 3 inches by 3 inches, rectangular, black, and mounted on a black wristband. SCUBAPRO is stamped on the top of the face frame and Aladin2 is printed in white on the bottom of the face frame. The serial number is stamped in white on the back of the unit and ends with 003.

Reason for Recall

The dive computer can leak and stop working, posing a risk of injury due to decompression sickness.

Remedy

Consumers should immediately stop using the dive computers and return them to an authorized SCUBAPRO dealer or contact Johnson Outdoors Diving for a free replacement.

Details

Units Affected
About 350 and about 40 in Canada
Official Source
https://www.cpsc.gov/Recalls/2014/Johnson-Outdoors-Diving-Recalls-Dive-Computers

Frequently Asked Questions

What product was recalled? ▼
This recall involves the Aladin2 wrist dive computer that monitors depth, dive time, decompression status and temperature. The computer is 3 inches by 3 inches, rectangular, black, and mounted on a black wristband. SCUBAPRO is stamped on the top of the face frame and Aladin2 is printed in white on the bottom of the face frame. The serial number is stamped in white on the back of the unit and ends with 003.. Recalled by Johnson Outdoors Diving Inc., of El Cajon, Calif.. Units affected: About 350 and about 40 in Canada.
Why was this product recalled? ▼
The dive computer can leak and stop working, posing a risk of injury due to decompression sickness.
What should consumers do? ▼
Consumers should immediately stop using the dive computers and return them to an authorized SCUBAPRO dealer or contact Johnson Outdoors Diving for a free replacement.
Which agency issued this recall? ▼
This recall was issued by the CPSC on August 5, 2014. Severity: Moderate. Recall number: 14249.

Related Recalls

FDA Devices Moderate

Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…

Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…

Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate

Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…

Fujirebio Diagnostics, Inc. · 2026-02-11

Explore Related Data

Vehicle Safety → Drug Information →