CPSCApril 2, 2003consumer
CPSC, Raven Industries Announce Recall of Handheld Remote Controls
Official recall recorded by the U.S. Consumer Product Safety Commission.
The hazard
An internal component can overheat, presenting risks of fire or thermal burns to consumers.
What to do
Consumers should stop using these remote controls immediately, contact Raven and mention the recall to receive a free replacement.
Brands named
infraredinfrared remotecpsccpsc raven
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAPhilips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual2025-11-26
- CPSCLifepro Fitness Recalls Bioremedy Infrared Sauna Blankets Due to Risk of Burn Injuries2025-10-23
- FDAInseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R2025-05-30
- FDATempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer), 00-1026-R (Tempus Pro printer, IBP), 00-1007 [(Tempus Pro, BT Dock (IB Only)], 00-1004 00-1004 [...2025-04-16
- FDAPhilips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-10072025-04-15
- FDATempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode2024-10-28
- FDAPhilips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual2024-05-09
- FDAPhilips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-20442023-08-24
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