Series OEC 9800. The Series OEC 9800 is designed to recall

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial No: 82-0013,82-0045,82-0061,82-0071,82-0085,82-0122,82-0133,82-0190,82-0246,82-0357,82-0528,82-0533,82-0597,82-0626,82-0699,82-0702,82-0707,82-0718,82-0805,82-0818,82-0854,82-0855,82-0946,82-1040,82-1052,82-1062,82-1106,82-1133,82-1199,82-1292,82-1324,82-1348,82-1411,82-1453,82-1460,82-1526,82-1542,82-1608,82-1651,82-1658,82-1679,82-1709,82-1731,82-1773,82-1822,82-1867,82-1882,82-1905,82-1914,82-1979,82-2017,82-2018,82-2024,82-2030,82-2036,82-2049,82-2165,82-2169,82-2206,82-2225,82-2241,82-2279,82-2356,82-2388,82-2398,82-2454,82-2455,82-2459,82-2474,82-2535,82-2565,82-2603,82-2650,82-2655,82-2735,82-2751,82-2761,82-2767,82-2783,82-2851,82-2855,82-2909,82-2930,82-2945,82-2975,82-3003,82-3094,82-3096,82-3169,82-3210,82-3226,82-3232,82-3241,82-3319,82-3325,82-3377,82-3389,82-3395,82-3406,82-3424,82-3430,82-3456,82-3459,82-3500,82-3523,82-3534,82-3539,82-3569,82-3571,82-3629,82-3713,82-3748,82-3774,82-3826,82-3837,82-3851,82-3895,82-7048-MH,82-7066-MH,82-7103-MH,89-0028,89-0034,89-0037,89-0072,89-0105,89-0113,89-0135-RC,89-0184,89-0192,89-0308,89-0311,89-0316,89-0318,89-0388,89-0396,89-0427,89-0517,89-0586,89-0600,89-0623,89-0624,89-0642,89-0643,89-0743,89-0825,89-0827,89-0840,89-0843,89-0846,89-0866,89-0881,89-0894,89-0930,89-0947,89-0995,89-1023,89-1145,89-1157,89-1202,89-1204,89-1209,89-1260,89-1308,89-1327,89-1375,89-1392,89-1408,89-1411,89-1544,89-1652,89-1671,89-1698,89-1751,89-1804,89-1849,89-1868,89-1956,89-1964,89-1984,89-1986,89-2031,89-2050,89-2083,89-2085,89-2094,89-2118,89-2142,89-2170,89-2199,89-2244,89-2250,89-2336,89-2354,89-2459,89-2550,89-2555,89-2598,89-2623,89-2674,89-2682,89-2690,89-2695,89-2767,89-2777,89-2850,89-2862,89-2900,89-3031,89-3032,89-3124-N,89-3165,89-3171,89-3222,89-3252,89-3254,89-3311,89-3318,89-3346,89-3359,89-3367,89-3368,89-3419,89-3438,89-3531,8S-0014-C,8S-0026,8S-0029,8S-0058,8S-0059,8S-0070,8S-0113,8S-0162,8S-0224,8S-0232,8S-0389,8S-0467,8S-0511,8S-0529,8S-0531,8S-0549,8S-0605,8S-0755,8S-0766,8S-0782,8S-0858,8S-0876,8S-0933-C,8S-0997,8S-1000,8S-1015,8S-1147,8S-1165,8S-1166,8S-1192,8S-1427,8S-1447,8S-1509-C,8S-1565,8S-1585,8S-1897,8S-1907,8S-2008-N,8S-2053,8S-2062,8S-2092,8S-2103,8S-2107,8S-2232,8S-2234,8S-2268,8S-2310,8S-2385,8S-2408,8S-2432,8S-2445,8S-2471-C,8S-2491,8S-2530,8S-2543,8S-2550,8S-2554,8S-2564,8S-2618,8S-2650,8S-2651,8S-2671,8S-2675,8S-2695,8S-2701,8S-2734,8S-2746,8S-2770,8S-2792,8S-2798,8S-2819,8S-2835,8S-2861,8S-2862,8S-2914,8S-2922,8S-2984,8S-3004,8S-3048,8S-3055,8S-3088,8S-3143,8S-3162-H,8S-3219,8S-3272-H,8S-3289-H,8S-7102-MH,

Product

Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient,during diagnostic, surgical and…

Recalling firm

GE OEC Medical Systems, Inc

Quantity

311

Distribution

Worldwide Distribution.

Recall date

November 19, 2014

Classification

Class II

Status

Terminated

Agency

FDA (device)