Recalls affecting District of Columbia

FDA has not published a risk classification for this recall yet.

Recall #:

79627

Lot/product code:

All Lots

Recalling firm:

Autochair

FDA has not published a risk classification for this recall yet.

Recall #:

78599

Lot/product code:

Product No. 160001  All Serial Numbers.

Recalling firm:

Hamilton Medical AG

FDA has not published a risk classification for this recall yet.

Recall #:

78599

Lot/product code:

Product No. 160005  All Serial Numbers

Recalling firm:

Hamilton Medical AG

FDA has not published a risk classification for this recall yet.

Recall #:

83268

Lot/product code:

All lots of RF assay

Recalling firm:

Hycor Biomedical Inc

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

F-1141-2018

Lot/product code:

GFS Product UPC 093901859372, Lot code: L1D1018, Best Before 09/06/19; Signature Select UPC 021130085460, Lot code: L1G1018, Best Before 09/07/19; Delizza UPC 676670001069; Lot code: L1M1018, Best Before 09/09/19

Recalling firm:

Poppies International INC

FDA has not published a risk classification for this recall yet.

Recall #:

80403

Lot/product code:

UDI: 00847865014151  Serial Numbers: 140600072,  160900991,  161001953,  1112001938,  1112001941 ,  1112004075 ,  1112004079 ,  1112004083 ,  1112004084 ,  1112004086 ,  1112004088 ,  1112004093 ,  1201003822 ,  1201003826 ,  1201003827 ,  1207001007 ,  1207001015 ,  1207001017 ,  1207001018 ,  1208001583 ,  1208001584 ,  1208001586 ,  1208001590 ,  1208005236 ,  1208005244 ,  1208005245 ,  1211000978 ,  1211000983 ,  1211006938 ,  1301003205 ,  1301003212 ,  1303000299 ,  1303000300 ,  1303000302 ,  1303000305 ,  1303007688 ,  1306003195 ,  1307006044 ,  1307006045 ,  1307006054 ,  1307006055 ,  1308000967 ,  1308000968 ,  1308000969 ,  1308000971 ,  1308000973 ,  1308003338 ,  1308003341 ,  1308003345 ,  1308003346 ,  1308006670 ,  1311008542 ,  1311008544 ,  1311008546 ,  1311008555 ,  1311008557 ,  1311008562 ,  1311008564 ,  1311008565 ,  1401002580 ,  1401002583 ,  1401002587 ,  1401007785 ,  1401007786 ,  1401007789 ,  1401007792 ,  1401007793 ,  1404000065 ,  1404000066 ,  1404000067 ,  1404000068 ,  1404002677 ,  1404002684 ,  1404002685 ,  1405005640 ,  1405005641 ,  1405005645 ,  1405005648 ,  1406000064 ,  1406000065 ,  1406000066 ,  1406000067 ,  1406000068 ,  1406000070 ,  1406000071 ,  1406000074 ,  1406006883 ,  1406006886 ,  1407004144 ,  1407004145 ,  1407004147 ,  1407004149 ,  1407004151 ,  1407004152 ,  1410010410 ,  1410010415 ,  1410010416 ,  1411010876 ,  1411010877 ,  1411010880 ,  1412001714 ,  1412001716 ,  1412001721 ,  1501001523 ,  1501001526 ,  1501001526 ,  1501005823 ,  1501005824 ,  1501005825 ,  1501005828 ,  1501005829 ,  1501005832 ,  1506008687 ,  1506008690 ,  1506008695 ,  1510005389 ,  1510005393 ,  1510005394 ,  1510005395 ,  1510005397 ,  1510005398 ,  1510005399 ,  1510005414 ,  1601001552 ,  1601001553 ,  1601001559 ,  1601001561 ,  1601001562 ,  1601001563 ,  1603001786 ,  1603005407 ,  1605000088 ,  1609000992 ,  1609000993 ,  1609000994 ,  1609000995 ,  1609000996 ,  1609001301 ,  1609001302 ,  1609001303 ,  1609001304 ,  1609001305 ,  1609001306 ,  1609009231 ,  1610001955 ,  1701001785 ,  1701001788 ,  1701004204 ,  1701004210 ,  1710010533 ,  1710010539 ,  13060003204 ,  16303005411 ,  s1411010876

Recalling firm:

Bio-Rad Laboratories Inc

FDA has not published a risk classification for this recall yet.

Recall #:

81459

Lot/product code:

Serial #17C0001 to #17C0252

Recalling firm:

Handpiece Headquarters

FDA has not published a risk classification for this recall yet.

Recall #:

79950

Lot/product code:

Lot 45016

Recalling firm:

MHC Medical Products LLC

FDA has not published a risk classification for this recall yet.

Recall #:

79950

Lot/product code:

Lot 45014

Recalling firm:

MHC Medical Products LLC

FDA has not published a risk classification for this recall yet.

Recall #:

80056

Lot/product code:

ALL SERIAL NUMBERS  UPN/GTIN: (a) 1400 and 1401: distributed prior to GTN requirement  1403: 00888707000116, 00888707000475  1407: '00888707000291, '00888707000727, '00888707000710,   00888707000734, '00888707000741, '00888707000765, '00888707000758, '00888707000789, '00888707000772, '00888707000499, '00888707000796, '00888707000802, '00888707000819, '00888707000482, '00888707004534, '0888707001670, '00888707001656, '00888707001663, '00888707001670, '00888707001687, '00888707001694, '00888707001700, '00888707001717, '00888707001724, '00888707001731, '00888707001748, '00888707001755, '00888707001762, '00888707002813, '00888707002820, '00888707002837, '00888707002844, '00888707002851, '00888707001472  1420: '00888707000420, '00888707000437, '00888707002660  (b) 1435: '00888707000109  1440: '00888707000260, '00888707001885, '00888707001496,  '00888707002745  (c) 1425: '00888707000093  1430: '00888707000307, '00888707000826, '00888707000833,  '00888707000840, '00888707000857, '00888707000871, '00888707000864,  '00888707000888, '00888707000901, '00888707000505, '00888707000895,  '00888707000918, '00888707001489, '00888707001779, '00888707001786,  '00888707001793, '00888707001809, '00888707001816, '00888707001823,  '00888707001830, '00888707001847, '00888707001854, '00888707001861,  '00888707001878, '00888707002738, '00888707002769, '00888707002776,  '00888707002783, '00888707002790, '00888707002806, '00888707004817  (d) 1650DE: 00888707000369, 00888707001373, '00888707001588, '00888707001366, '00888707002684 '00888707002646, '00888707002653,  '00888707000376

Recalling firm:

Heartware

FDA has not published a risk classification for this recall yet.

Recall #:

80003

Lot/product code:

All Serial Numbers distributed from 03/06/2012 to 04/26/2018

Recalling firm:

Maquet Datascope Corp - Cardiac Assist Division

FDA has not published a risk classification for this recall yet.

Recall #:

80691

Lot/product code:

UDI Number: 00886874114193. Serial Number: SK1703.

Recalling firm:

Intuitive Surgical, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L1049X & N7M0723X

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L0823KX, N8A0799KX & N8B1008KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L0551KX & N7M0877KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L1019X, N7M0129X & N7L0734X

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N8A0146KX, N8A0327KX & N8A0907KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L0521KX, N7M0047KX, N7M0592KX, N7M1001KX, N7L0975KX, N7M0434KX, N7M0683KX, N8A0203KX, N7L1057KX, N7M0528KX, N7M0937KX, N8A0677KX, N7L1098KX, N7M0529KX, N7M0949KX, N8C0144KX & N7L1099KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L0852X, N7M0130X, N8A0145X, N8A0336X, N7L0931X, N7M0639X, N8A0796X & N8B0993X

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L0915X & N7M0468X

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7M0045KX, N7M0398KX, N8A0523KX, N8B0088KX, N7M0070KX, N8A0255KX & N8B0080KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L1163X & N7M0156X

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7G0756KX & N7L0819KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L0974KX, N7M0486KX, N7M0762KX & N8A0363KX

Recalling firm:

COVIDIEN MEDTRONIC

FDA has not published a risk classification for this recall yet.

Recall #:

80423

Lot/product code:

N7L1041KX & N8A0199KX

Recalling firm:

COVIDIEN MEDTRONIC