Devices

Device Recall DePuy ASR 100 Acetabular Implant, 62 mm

Model / Serial
1118116, 1118118, 1976202, 1976203, 1976204, 1998484, 1998485, 2009838, 2009839, 2009840, 2009841, 2062931, 2062932, 2062933, 2062934, 2082770, 2082771, 2082772, 2082773, 2117373, 2117374, 2117375, 2117376, 2125498, 2125499, 2125500, 2141310, 2141311, 2141312, 2147434, 2147435, 2158478, 2158479, 2158480, 2159204, 2159205, 2165159, 2165160, 2169673, 2169674, 2169675, 2189090, 2189091, 2189092, 2189093, 2191205, 2191206, 2191207, 2204187, 2204188, 2281763, 2281764, 2284515, 2299846, 2326671, 2326672, 2332883, 2345853, 2345854, 2353986, 2353987, 2377624, 2410563, 2410564, 2416135, 2416136, 2437528, 2437529, 2452466, 2452467, 2452468, 2464125, 2464126, 2538499, 2538500, 2555974, 2555975, 2571534, 2571535, 2571536, 2583606, 2583608, 2583609, 2596554, 2596555, 2596556, 2615391, 2615392, 2615393, 2617505, 2649161, 2649162, 2650300, 2679862, 2762657, 2762658, 2762659, 2762660, 2864933, 2864934, Y28JC1 and Y3TH31000.
Product Classification
Orthopedic Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide
Product Description
DePuy ASR 100 Acetabular Implant, 62 mm, 999800762, sterile, DePuy International, Ltd, Leeds, United Kingdom.
Manufacturer
Depuy Orthopaedics, Inc.
1 Event
- Recall of Device Recall DePuy ASR 100 Acetabular Implant, 62 mm

Manufacturer

Depuy Orthopaedics, Inc.

Manufacturer Address
Depuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
Source
USFDA

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