Salter Labs Recalls
5 recalls on record · July 4, 2012 to February 17, 2016 · Medical Devices
Recalls by year
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14
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 17, 2016Medical DevicesFDA
Salter Labs recalls T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device d
Hazard: Reports that the T-piece does not fit on the nebulizer.
September 23, 2015Medical DevicesFDA
Salter Labs recalls NebuTech Nebulizer, Model number: Series 8660, 8960, 8961, 8966, 8984. Nebulizer used to generate aerosols delivered dir
Hazard: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and may detach before or during treatment.
July 30, 2014Medical DevicesFDA
Salter Labs recalls Oxygen Mask, Model No. 8120-7 Product Usage: Oxygen Mask, High Concentration partial rebreather, with 7 foot (2.1 m)
Hazard: The case label correctly states partial rebreather but the insert label incorrectly states non-rebreather.
November 27, 2013Medical DevicesFDA
SALTER LABS recalls Salter Labs EtCO2 Sample line 15' (4.6 M) tube, male luer connectors. Rx only; Made in Mexico; Manufacturer:Salter Labs
Hazard: It has been determined that three lots of model number 4515-15-25 CO2 Sample Line 15' tube, male Luer lock connectors may contain a 30' tube instead of the 15' length.
July 4, 2012Medical DevicesFDA
SALTER LABS recalls Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For
Hazard: A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector actually contained product with a female luer lock connector.