Vial2BAG DC 20mm: 1) recall
Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use only, Rx Only
Why was Vial2BAG DC 20mm: 1) recalled?
Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag DC 20mm is recalled due to similarities with 13mm Vial2Bag DC.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
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?
UDI: (01)07290108240054(17)190101(10)7689(90)36098126(91)6070112 Lot Numbers: 7689, 7690, 7750, 7751, 7865, 7866, 7867, 7868, 7886, 7887, 7888, 7900, 7901, 7902, 7957, 7958, 7959, 7960, 7949, 7951, 7952, 7954, 8019, 8020, 8021, 8022, 8132, 8133, 8134, 8135, 8136, 8137, 8138, 8139, 8140, 8141, 8142, 8143, 8144, 8145, 8147, 8148, 8149, 8150, 8151, 8470, 8471, 8472, 8473, 8483, 8696, 8553, 8554, 8555, 8556, 8557, 8558, 8559, 8560, 8561, 8562, 8563, 8564, 8565, 8566, 8567, 8568, 8569, 8570, 8571, 8760, 8761, 8762, 8763, 8764, 8765, 8766, 8767, 8768, 8769, 8770, 8771, 8772, 8887, 8888, 8889, 8890, 8891, 8892, 8893, 8894, 8895, 9040, 9041, 9042, 9042, 9043, 9044, 9045, 9046, 9047, 9169, 9170, 9171, 9172, 9173, 9174, 9271, 9272, 9273, 9274, 9275, 9276, 9277, 9278, 9323, 9324, 9325, 9326, 9327, 9328, 9329, 9330, 9394, 9500, 9501, 9502, 9503, 9504, 9505, 9506, 9507, 9508, 9509, 9510, 9511, 9512, 9513, 9514, 9515, 9529, 9530, 9531, 9532, 9533, 9534, 9535, 9537, 9560, 9561, 9562, 9563, 9564, 9565, 9566, 9567, 9568, 9569, 9570, 9571, 9572, 9657, 9658, 9659, 9660, 9661, 9662, 9663, 9664, 9665, 9666, 9667, 9668, 9717, 9718, 9719, 9720, 9721, 9722, 9723, 9724, 9725, 9726, 9727, 9728, 9729, 9730, 9810, 9841, 9842, 9843, 9844, 9845, 9846, 9847, 9848, 9849, 9964, 9965, 9966, 9967, 9968, 9969, 9970, 9971, 9972, 9973, 9974, 9975, 9976, 9978, 9979, 9980, A018, A019, A001, A002, A003, A004, A005, A020, A021, A022, A023, A024, A025, A026, A027, A028, A029, A030, A031, A032, A033, A034, A006, A007, A008, A009, A010, A011, A012, A013, A014, A015, A016, A017, A106, A107, A108, A109, A110, A111, A258, A112, A113, A114, A115, A116, A117, A118, A119, A120, A121, A122, A254, A321, A322, A323, A330, A343, A344, A345, A346, A347, A348, A349, A350, A351, A352, A353, A354, A355, A324, A325, A326, A327, A328, A329, A331, A332, A333, A334, A335, A336, A337, A356, A357, A358, A359, A360, A361, A362, A338, A339, A340, A519, A520, A521, A522, A523, A524, A525, A526, A527, A528, A529, A530, A530, A531, A532, A533, A534, A535, A536, A537, A538, A539, A540, A541, A542, A543, A544, A545, A546, A547, A548, A549, A550, A551, A552, A553, A554, A555, A556, A557, A558, A559, A560, A561, A562, A563, A564, A565, A566, A568, A569, A570, A571, A572, A567, A573, A574, A575, A576, A577, A578, A579, A580, A581, A582, A817, A819, A813, A814, A815, A816, A818, A820, A821, A822, A823, A824, A825, A826, A840, A840, A841, A842, A843, A843, A845, A844, A898, A899, A900, A901, A902, A903, A904, A905, A906, A907, A908, A909, A910, A911, A915, A916, A917, A918, A919, A920, A921, A982, A983, A984, A985, A986, A987, A988, C015, C016, C017, C017, C033, C034, C035, C036, C037, C038, C039, C040, C041, C042, C043, C044, C045, C046, C047, C048, C049, C050, C051, C052, C053, C054, C055 & C056 UDI: (01)07290108241006(17)190501(10)8344(90)36098138(91)6070112C Lot Number: 8344
- Product
- Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use only, Rx Only
- Recalling firm
- WEST PHARMA. SERVICES IL, LTD
- Quantity
- 30 million units
- Distribution
- US Distributor in MO
- Recall date
- February 6, 2019
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)