Recalls affecting Michigan

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

Recall #:

85034

Lot/product code:

1134117 1101918 1107518 1114918 1121118 1127718 1131018 1133218 1135118 1105919 1118819 1121419 1124919

Recalling firm:

Gentell, Inc

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

Recall #:

85309

Lot/product code:

Serial Numbers: AGB1692005, AGB17Z2010, AGA1552003, AGB17Y2009, AGB1682004, AGA1492002, AGC1822012, A5C1922001, AGB1712007, AGC1952014, AGB1482001, AGC1822011, BGB1992001, AGC18X2013, AGB16Z2006

Recalling firm:

Canon Medical System, USA, INC.

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

Recall #:

85309

Lot/product code:

Serial Numbers: B8B1972001, A9A1592001, A3A14Z2001, AEB1812002, A1B1552001, A9C18Y2007, A3E1922002, B5B1952001, A9C1822006, A9B1622002, A9B1722003, A5C1622001, B3B19Y2001, A1D1772003, B1B19X2001, A5C16Y2002, A9C1822005, A1E1862008, A1D1752002, A1E1832004, A1E1852005, A1E1852006, A5E1862003, AEA17X2001

Recalling firm:

Canon Medical System, USA, INC.

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

Recall #:

85309

Lot/product code:

Serial Numbers: A5B1642006, A1B17X2004, A5A1612005, A5B1772009, B5B1962002, A3A1522004, A7B16Y2001, A3A1712011, A5B1792010, A5A1532002, A1A1612003, A3A15Z2007, A5A1552003, A5B16Y2007, A3B1862016, A3B1812013, A3A1662009, A9A16X2004, BTA1922001, A3B1842015, AOB1882001, BMB1942001, AOB1892002, A5B1472001, A5B17Z2011, A3A14X2002, A5A1592004, A3A17Z2012, A5C1832012, A5B16Z2008, A1A1582002, A9A1582002, A1A14X2001, A3A1512003, A7C1812002, ABC18X2002, A3A1592005, UTC14Y2008, A3A15X2006, B5B1942001, A3A1682010, A1C18Z2005, A9A1662003, A3A1492001, A3B1822014, A3A1622008

Recalling firm:

Canon Medical System, USA, INC.

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

Recall #:

85255

Lot/product code:

Systems with software versions: 4.0.0.14 , 4.0.1.4 , 4.0.2.9 , 4.0.3.4 , 4.5.0.19 , 4.5.1.14 , 4.5.2.7 , 4.7.0.15 , 4.7.1.10 , 4.7.2.5 , 4.7.3.13 , 4.7.4.4 , 4.7.5.4 , 4.7.6.7 , 4.9.0.42 , 5.0.0.37 , 5.0.1.11 , 5.0.2.35 , 5.0.3.17 , 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 or 9.1.0.933

Recalling firm:

RAYSEARCH LABORATORIES AB

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

Recall #:

85113

Lot/product code:

Serial Numbers: 100002908 to 100027093; 100027096 to 100085389; 100085399 to 100109746; 100109868 to 201003390; 201003392 to 201010952

Recalling firm:

Respironics California, LLC

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

Recall #:

85252

Lot/product code:

Serial Numbers: 1507T719-00-0-0087 1509T719-00-0-0142 1509T719-00-0-0144 1509T719-00-0-0139 1507T719-00-0-0085 1509T719-00-0-0135 1508T719-00-0-0115 1508T719-00-0-0116 1508T719-00-0-0119 1508T719-00-0-0120 1507T719-00-0-0074 1508T719-00-0-0129 1508T719-00-0-0121 1508T719-00-0-0123 1508T719-00-0-0124 1508T719-00-0-0125 1508T719-00-0-0126 1509T719-00-0-0132 1509T719-00-0-0146 1507T719-00-0-0103 1507T719-00-0-0104 1507T719-00-0-0053 1507T719-00-0-0054 1507T719-00-0-0055 1507T719-00-0-0056 1507T719-00-0-0058 1507T719-00-0-0059 1507T719-00-0-0061 1507T719-00-0-0062 1507T719-00-0-0063 1507T719-00-0-0064 1508T719-00-0-0127 1508T719-00-0-0128 1510T719-00-0-0153 1510T719-00-0-0154 1510T719-00-0-0157 1510T719-00-0-0160 1510T719-00-0-0166 1508T719-00-0-0118 1510T719-00-0-0159 1508T719-00-0-0114 1508T719-00-0-0117 1508T719-00-0-0122

Recalling firm:

Skytron, Div. The KMW Group, Inc

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

Recall #:

85094

Lot/product code:

Model Number 4BCPPB-3XCZ0002 (Lot Numbers PPB1155 - PPB1174, PPB1194 - PPB1213, PPB1222 - PPB1241, PPB1265 - PPB1284, PPB1292 - PPB1311, PPB1346 - PPB1365, PPB1375 - PPB1394, PPB1451 - PPB1466, PPB1477 - PPB1496, PPB1508 - PPB1527);   Model Number 4BCPPB-CCZ0008, Lot Number PPB1446 - PPB1449;  Model Number 4BCPPB-BCZ0009, Lot Number PPB1541 - PPB1542

Recalling firm:

Linet Americas

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24538844, 24647121

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24423656, 24423820, 24424087, 24427952, 24427959, 24428330, 24430010, 24437882, 24440182, 24440998, 24444952, 24446611, 24447516, 24447658, 24447722, 24447735, 24451828, 24452126, 24452132, 24452266, 24454238, 24455297, 24455381, 24455732, 24460452, 24460458, 24466032, 24487805, 24493956, 24494611, 24498583, 24498730, 24498732, 24499924, 24501439, 24506583, 24563429, 24563891, 24564727, 24564729, 24569684, 24570465, 24571203, 24579763, 24599358, 24609013, 24609991, 24614307, 24615296, 24620493, 24621357, 24621789, 24622541, 24623111, 24623117, 24623321, 24623461, 24623472, 24640257, 24661651, 24662199, 24663152, 24663562, 24663570, 24665001, 24665005, 24665100, 24665108, 24665990, 24666401, 24670677, 24672232, 24672553, 24678045, 24678047, 24681044, 24699798, 24700605, 24702016, 24708365, 24708371, 24709540, 24709550, 24710261, 24716280, 24716623, 24719303, 24723783, 24724284, 24732445, 24732731, 24738283, 24751717, 24756104, 24758578, 24763250, 24765356, 24766287, 24766401, 24772737, 24773528

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24484631, 24494135, 24494288, 24533782, 24584655, 24617736, 24625474, 24665994, 24723912

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24795838

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24501748, 24506585, 24507390, 24507747, 24517205, 24517209, 24517211, 24526341, 24576484, 24576569, 24577900, 24579133, 24580102, 24583255, 24585905, 24586401, 24616721, 24617337, 24618334, 24724936, 24732742, 24737184, 24739802, 24790717, 24805720, 24860825, 24868932

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24724232

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Number: 24958079 (edited 1/13/2021)

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24879999, 25021676

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Number: 24835477 (edited 1/13/2021)

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24749818, 24913418

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24755840

Recalling firm:

Boston Scientific

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

Recall #:

85227

Lot/product code:

Lot Numbers: 24755842

Recalling firm:

Boston Scientific

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

Recall #:

85209

Lot/product code:

VITEK 2AST-P652 Test Kit with Catalog #421857 and Lot# 8021232403 Manufactured 11OCT2019, Expires 11APR2021

Recalling firm:

Biomerieux Inc

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

Recall #:

85310

Lot/product code:

All serial numbers

Recalling firm:

Fresenius Medical Care Holdings, Inc.

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

Recall #:

85310

Lot/product code:

All serial numbers

Recalling firm:

Fresenius Medical Care Holdings, Inc.

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

Recall #:

85270

Lot/product code:

LOT K030.

Recalling firm:

Rayner Intraocular Lenses Limited

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

Recall #:

85296

Lot/product code:

Lot Numbers: 2013889 2013916 2013955 2014296 2016197 2016198 2016232 2016233 2016234 2017395 2017761 2017818 2017819 2018639 2018801 2018855 2019841 2019893 2019992 2021327 2021390 2021391 2021499 2022264 2022265 2022266 2022267 2024809 2025064 2025065 2025165 2025169 2025343 2025386 2027398 2027429 2028620 2029251 2029252 2029253 2029254 2029295 2029296 2029297 2029298 2029337 2029338 2029339 2029340 2029386 2029387 2030937 2030938 2030939 2030940 2031077 2031078 2031079 2031080 2031145 2032812 2032813 2032814 2032815 2033272 2033273 2033387 2033388 2033389 2033390 2033391 2033517 2033518 2033519 2033520 2033521 2033522 2033523 2033524 2033525 2033526 2033527 2033528 2033664 2034417 2034418 2034482 2034483 2036298 2036299 2036704 2036705 2037123 2037124 2037125 2037171 2037176 2038315 2038316 2038449 2038452 2038785 2038786 2038787 2038788 2038919 2039245 2039247 2039436 2039437 2039438 2040097 2040098 2040099 2040100 2040101 2040727 2040728 2040729 2041051 2041052 2041053 2041054 2041055 2041194 2041195 2041196 2041197 2041198 2041780 2041781 2041782 2042582 2042583 2042584 2042763 2042764 2042765 2044884 2044885 2044886 2044887 2044888 2045848 50532035 50598665 50670645 50721923 50721924 50722153 50722409 50723724 50723725 50723729 50724822 50725155 50725156 50726258 50726558 50726559 50730869 50730870 50730871 50730872 50730876 50730877 50734025 50734026 50734031 50734035 50734038 50734041 50736231 50736234 50737178 50737941 50737942 50738087 50738088 50738894 50738895 50738896 50742394 50742585 50742586 50744052 50744053 50744054 50744777 50745439 50745440 50745441 50746623 50746624 50746625 50747145 50747146 50747859 50747860 50748081 50748082 50748083 50748084 50751684 50753515 50753518 50760611 50760612 50760613 50760614 50760802 50760803 50760805 50760806 50760807 50766818 50766828 50769166 50769167 50769168 50773888 50774344 50776630 50776631 50785146 50785147 50785261 50785262 50785263 50785505 50785506 50793871 50795930 50795933 50795936 50803204 50803205 50807430 50807431 50811207 50811209 50815810 50815812 50821889 50821892 50831271 50831742

Recalling firm:

Smith & Nephew, Inc.