FDAJanuary 27, 2017device
Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The wiring may allow the lamps to turn on with the key switch rather than the timer.
What to do
FDA enforcement status: Terminated
Brands named
national biologicalnational
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDAEdge Biologicals STERILE WATER, 3ML, 100/PK CAT T-0780 Sterile Water, 3mL, 10/PK - Sterile water is used in making dilutions of samples/transport media in preparation for microbial testing of the sample. It is also used for diluting sterile reagents and microorganism preparations2023-10-02
- CPSCCPSC, thyssenkrupp Access Corp. Settle Lawsuit: Firm to Conduct Recall to Inspect Home Elevators Due to Entrapment Hazard Posing Risk of Serious Injury or Death to Children; One Child Death Reported2022-09-14
- FDAECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Ultrasound Transmission Clr 8.5 oz BTL 24/cs ECO 40JMC Gel Ultrasound Transmission Clr 5L 4/cs NDC P301008 ProAdvantage Gel Ultrasound Transmission 8.5 oz 12/cs NDC P301105 ProAdvantage Gel Ultrasound Transmission 5 Liter 4/cs NDC P301115 ProA...2021-08-24
- FDAECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl2021-08-24
- CPSCNational Presto Recalls Smokers Due to Electric Shock Hazard2021-02-17
- FDAFrozen French Cut Green Beans. Packaged in 20.5 lb boxes. Expiration date 11/25/20222020-10-28
- FDANature's Blend Folic Acid 1000 mcg Dietary Supplement, 1000-count bottle, Product Number: 1280, UPC 0-79854-51280-92020-02-28
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