Recall of Device Recall Olympic Pasteurmatic 3000; Olympic Pasteurmatic 3500

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Natus Medical Incorporated.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    76427
  • Event Risk Class
    Class 2
  • Event Number
    Z-2701-2017
  • Event Initiated Date
    2017-05-22
  • Event Date Posted
    2017-06-02
  • Event Status
    Open, Classified
  • Event Country
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Disinfector, medical devices - Product Code MEC
  • Reason
    Olympic pasteurmatic 3000/3500 systems are recalled because they do not fully meet todays regulatory requirements. given the age of the products design, component and technology obsolescence, and the time involved in fully complying with the latest design and development standards, the firm decided to recall of the olympic pasteurmatic 3000/3500 system devices by means of disabling the devices.
  • Action
    Natus Medical sent an URGENT: RECALL NOTIFICATION MEDICAL DEVICE RECALL letter dated May 2017. Please refer to the accompanying Instructions to Disable the Pasteurmatic (DOC-022838), then complete and return the attached reply form. Should you require assistance in decommissioning your affected system please indicate option 2 on the reply form and you will be contacted to schedule an in- service. Natus may reimburse facilities for Olympic Pasteurmatic" 3000/3500 System purchases based on the age of the affected system as determined by the system serial number. There is no evidence to suggest there is a safety risk associated with the Olympic Pasteurmatic" 3000/3500 System device, nor have there been any safety incidences reported to Natus. Natus apologizes for any inconvenience. Please understand that this is part of our commitment to providing only the highest quality products and information to our customers. Please contact us at Natus_Quality_Programs@natus.com or (866) 940-7143 option #2 if you have any further questions.

Device

  • Model / Serial
    ************Serial numbers of affected units distributed to US government***************  3056 and 9199.  ************Serial numbers of affected units distributed to US consignees***************  3039, 3041, 3043, 3045, 3050, 3055, 3062, 3071, 3079, 3083, 3084, 3096, 3100, 3113, 3143, 3153, 3155, 3162, 3165, 3174, 3188, 3192, 3194, 3195, 3223, 3224, 3229, 3232, 3238, 3240, 3249, 3260, 3265, 9197, 9198, 03003, 03004, 03012, 03020, 03022, 03028, 03034, 03047, 3002, 3006, 3009, 3013, 3029, 3035, 3044, 3046, 3047, 3048, 3052, 3059, 3063, 3084, 3085, 3091, 3091, 3094, 3099, 3101, 3110, 3118, 3134, 3136, 3142, 3145, 3148, 3149, 3156, 3161, 3169, 3171, 3173, 3180, 3181, 3183, 3185, 3189, 3190, 3198, 3225, 3227, 3237, 3239, 3241, 3266, 3277, 3278, 3279, 3281, 3345, and 9198.   ************Serial numbers of affected units distributed to international consignees*******  3019, 3036, 3040, 3049, 3051, 3053, 3054, 3057, 3061, 3064, 3065, 3067, 3072, 3073, 3074, 3077, 3078, 3080, 3081, 3082, 3083, 3084, 3086, 3087, 3088, 3089, 3090, 3092, 3093, 3097, 3098, 3102, 3103, 3104, 3106, 3107, 3109, 3113, 3116, 3117, 3120, 3123, 3124, 3129, 3130, 3131, 3132, 3135, 3137, 3138, 3139, 3144, 3146, 3147, 3150, 3151, 3152, 3154, 3158, 3163, 3164, 3166, 3167, 3172, 3172, 3175, 3177, 3178, 3179, 3182, 3186, 3187, 3193, 3196, 3204, 3206, 3208, 3210, 3211, 3211, 3215, 3217, 3218, 3219, 3220, 3221, 3222, 3226, 3228, 3230, 3231, 3233, 3234, 3235, 3242, 3243, 3244, 3245, 3246, 3247, 3250, 3251, 3252, 3253, 3254, 3257, 3261, 3264, 3267, 3268, 3269, 3270, 3272, 3273, 3274, 3276, 3280, 03008, 03014, 03017, 03018, 03021, 03023, 03024, 03027, 03175, 03200, 3025, 3035, 3037, 3058, 3060, 3068, 3070, 3075, 3076, 3095, 3105, 3108, 3111, 3114, 3115, 3119, 3121, 3122, 3125, 3126, 3128, 3133, 3140, 3141, 3157, 3159, 3160, 3168, 3170, 3176, 3184, 3191, 3200, 3201, 3202, 3203, 3205, 3207, 3209, 3212, 3213, 3214, 3216, 3236, 3248, 3258, 3259, 3262, 3271, 3275, and 9200.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) Distribution to the states of : AL, AR, CA, CO, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, WI, and WV and in the following countries: Canada, Colombia, Costa Rica, Ecuador, Hong Kong, India, Indonesia, Japan, Korea, Malaysia, Mexico, Panama, Peru, Qatar, Saudi Arabia, Taiwan, Thailand, and Viet Nam.
  • Product Description
    The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of respiratory therapy and anesthesia equipment by killing vegetative bacteria and viruses, in a hot water bath at ~160¿ - ~170¿ F for 30 minutes. || Catalog Number/Description: || 007168 PM3500 ASSY (15KW 208/120V) || 007169 PM3000 ASSY (9KW 208/120V) || 007169R PM3 (9KW 208/120) REFURB || 007170 PM3 ASSY (8.3KW 200V DELTA) || 007171 PM3 ASSY (9KW 220V SING PH) || 52640 PASTEURMATIC 3000 W/O BASKETS || 52640R PM 3000 w/o Baskets Refurb || 52640-200 PM 3000 W/O BASKETS 200V || 52640-220 PM 3000 W/O BASKETS 220V || 52641 PASTEURMATIC 3000 W/BASKET S || 52641R PM 3000 w/ Baskets Refurb || 52641-200 PM 3000 W BASKETS 200V || 52641-220 PM 3000 W/ BASKETS 220V || 52650 PASTEURMATIC 3500 W/O BASKET || 52651 PASTEURMATIC 3500 W/BASKETS S
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Natus Medical Incorporated, 5900 1st Ave S, Seattle WA 98108-3248
  • Manufacturer Parent Company (2017)
  • Source
    USFDA