Recalls affecting Oklahoma

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

Recall #:

88586

Lot/product code:

(1) REF 1882916, GTIN/UPN 20763000041223 - Lot/serial numbers 0217968715, 0218283722, 0218283942, 0218356873, 0218356874, 0218356875, 0218623544, 0219369113, 0219501397, 0219700166, 0220118673, 0220659645, 0220784922, 0220826101, 0220826102, 0221020300, 0221118606, 0221118607, 0221118608, 0221198946, 0221198951, 0221198952, 0221430166, 0221489935, 0221611652, 0221791819, 0221791821; (2) REF 1883514, GTIN/UPN 20763000040967 - Lot/serial numbers 0218283532, 0218791333, 0219215919; (3) REF 1884013, GTIN/UPN 20763000041230 - Lot/serial numbers 0217969616, 0217969617, 0218283944, 0218572177, 0219010745, 0219110914, 0221170726, 0221603993, 0221783424, 0221791809; (4) REF 1884020, GTIN/UPN 20763000040301 - Lot/serial numbers 0219501396, 0220648062, 0220649166, 0220892207, 0221156835, 0221271500; (5) REF 1884032, GTIN/UPN 00763000036140 - Lot/serial numbers 0220057395, 0220057397; (6) REF 1884033, GTIN/UPN 00763000036447 - Lot/serial numbers 0220057389, 0220057390, 0220057392; (7) REF 1882902HRE, GTIN/UPN 00763000036720 - Lot/serial numbers 0217969607, 0218283720, 0218283721, 0219215912, 0219435041, 0221527810, 0221969518; (8) REF 1882905HRE, GTIN/UPN 00763000036782 - Lot/serial numbers 0217968718, 0217968719, 0218283717, 0218283719, 0218356097, 0218790225, 0219215913, 0220177024, 0220659109, 0220659110, 0220878176, 0221091604, 0221091605, 0221118614, 0221258284, 0221527812, 0221611654; (9) REF 1882924HRE, GTIN/UPN 00763000036744 - Lot/serial numbers 0220057236, 0220057237, 0220057238, 0220057239, 0220057241, 0220057242, 0220057243, 0220057244, 0220560777, 0220659671, 0220878169, 0221072336, 0221156836, 0221275006, 0221611653, 0221619324, 0221791822; (10) REF 1882936E, GTIN/UPN 00763000036799 - Lot/serial numbers 0218377217, 0219660525; (11) REF 1882937E, GTIN/UPN 00763000036805 - Lot/serial numbers 0218377221, 0219661147, 0221279640; (12) REF 1882979HRE, GTIN/UPN 00763000033552 - Lot/serial numbers 0217970486, 0217970490, 0218162629, 0218547894; (13) REF 1883080HRE, GTIN/UPN 00763000033989 - Lot/serial numbers 0217261083, 0217261084, 0217261085, 0218354891, 0218421177, 0218790160, 0219036457; (14) REF 1883480HRE, GTIN/UPN 00763000033996 - Lot/serial numbers 0217261083, 0217261084, 0217261085, 0218354891, 0218421177, 0218790160, 0219036457; (15) REF 1883502HRE, GTIN/UPN 00763000036713 - Lot/serial numbers 0217666178, 0217666179, 0218356088, 0218356089, 0218790221, 0219215911, 0219435040, 0220929595, 0221072335, 0221110715, 0221110717, 0221118531, 0221182357, 0221468015; (16) REF 1883506HRE, GTIN/UPN 00763000037376 - Lot/serial numbers 0217666180, 0217666181, 0217667208, 0218356103, 0218790743, 0219728474, 0220070439, 0220118669, 0220158600, 0220484568, 0221119048, 0221258278, 0221468019, 0221611257, 0221611258; (17) REF 1883512HRE, GTIN/UPN 00763000037369 - Lot/serial numbers 0218356098, 0218356099, 0218356100; (18) REF 1883516HRE, GTIN/UPN 00763000037383 - Lot/serial numbers 0217665427, 0217665428, 0217665429, 0217666173, 0217666174, 0217666175, 0217666176, 0217666177, 0218572169, 0219699597, 0219728468, 0219728469, 0219848777, 0219848778, 0219848779, 0219859949, 0220124591, 0220124592, 0220124593, 0220266094, 0220313525, 0220313606, 0220313607, 0220313608, 0220313609, 0220313610, 0220313611, 0220313612, 0220484569, 0220484570, 0220891745, 0220892206, 0221111087, 0221111089, 0221111092, 0221111093, 0221118545, 0221261887, 0221271501, 0221279626, 0221279627, 0221477061, 0221477062, 0221477063, 0221477064, 0221611647, 0221611648, 0221611649, 0221791908, 0221791910, 0221791911; (19) REF 1884005HRE, GTIN/UPN 00763000036737 - Lot/serial numbers 0217968722, 0218161789, 0218161790, 0218356090, 0218790222; (20) REF 1884030HRE, GTIN/UPN 00763000036751 - Lot/serial numbers 0219968104, 0220031839, 0220031841, 0220031842, 0220031843, 0220484572, 0220560783, 0221118618, 0221258283, 0221468017, 0221698794, 0222008093; (21) REF 1884031HRE, GTIN/UPN 00763000036768 - Lot/serial numbers 0219968105, 0220032167, 0220032168, 0220032169, 0220468850, 0220583927, 0220934514, 0221072334, 0221279641, 0221792010, 0222008095; (22) REF 1884033HRE, GTIN/UPN 00763000036775 - Lot/serial numbers 0220057245, 0220057386, 0220057387; (23) REF 1884380HR, GTIN/UPN 20763000038162 - Lot/serial numbers 0217261579, 0217261580, 0217261581, 0217261582, 0217911696, 0217911698, 0217968713, 0218283533, 0218356295, 0218356302, 0218356303, 0218356304, 0218356305, 0218356866, 0218356867, 0218356870, 0218356871, 0218356872, 0218404708, 0218404710, 0218572170, 0218572171, 0218572172, 0218572173, 0218572174, 0218572175, 0218653925, 0218655886, 0218655887, 0218655888, 0218790744, 0218790745, 0218791326, 0218791327, 0218791328, 0218791329, 0218791330, 0218791331, 0218791332, 0219215917, 0219423535, 0219488214, 0219488215, 0219488216, 0219488217, 0219488218, 0219501398, 0219501399, 0219501400, 0219501401, 0219550301, 0219556484, 0219568999, 0219569000, 0219569001, 0219594771, 0219594772, 0219594773, 0219619651, 0219632566, 0219632567, 0219679070,… (truncated, 6050 characters total — see the official FDA record for the full value)

Recalling firm:

Medtronic Xomed, Inc.

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

Recall #:

88586

Lot/product code:

(1) REF 40A2500, GTIN/UPN 00763000033835, Lot/serial number 0220002825; (2) REF 40R2000, GTIN/UPN 00763000033866, Lot/serial number 0218179458; (3) REF 40R2500, GTIN/UPN 00763000033798, Lot/serial number 0218299192; (4) REF 40S2000, GTIN/UPN 00763000033873, Lot/serial number 0218179459; (5) REF 40S2500, GTIN/UPN 00763000043193, Lot/serial number 0220226674; (6) REF 45A2000, GTIN/UPN 00763000033880, Lot/serial number 0220443669; (7) REF 45A2500, GTIN/UPN 00763000043223, Lot/serial number 0218323602; (8) REF 45R2000, GTIN/UPN 00763000033897, Lot/serial numbers 0218284087, 0218292178, 0218973633; (9) REF 45R2500, GTIN/UPN 00763000033811, Lot/serial number 0218297618; (10) REF 45S2000, GTIN/UPN 00763000033903, Lot/serial number 0218299193; (11) REF 45S2500, GTIN/UPN 00763000043216, Lot/serial number 0218297619.

Recalling firm:

Medtronic Xomed, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

D-0005-2022

Lot/product code:

Lot # CB21024, Exp 2/2023

Recalling firm:

RISING PHARMACEUTICALS

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88683

Lot/product code:

serial numbers 22689696 through 23569078

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88599

Lot/product code:

MOSAIQ 2.83 when run with First Data Bank (FDB), UDI/GTIN MOSAIQ 2.83 (0858164002367)

Recalling firm:

Elekta, Inc.

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

Recall #:

D-0814-2021

Lot/product code:

Lot #: UV1335; UV1352; and UV1373

Recalling firm:

Morton Grove Pharmaceuticals, Inc.

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

Recall #:

D-0816-2021

Lot/product code:

Lot #: UV1159

Recalling firm:

Morton Grove Pharmaceuticals, Inc.

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

Recall #:

88607

Lot/product code:

All lot numbers

Recalling firm:

Roche Molecular Systems, Inc.

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

Recall #:

88501

Lot/product code:

Software versions 2.1.0-2.3.0, Serial numbers 116280503226 thru 121250000503 manufactured from 01-July-2016 thru 01-Jul-2021.

Recalling firm:

Welch Allyn Inc Mortara

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

Recall #:

D-0815-2021

Lot/product code:

Lot #: UV1198

Recalling firm:

Morton Grove Pharmaceuticals, Inc.

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

Recall #:

88623

Lot/product code:

All Lots Manufactured by Eco-Med Pharmaceutical, Inc

Recalling firm:

DJO, LLC

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

Recall #:

88623

Lot/product code:

All Lots manufactured by Eco-Med Pharmaceutical, Inc

Recalling firm:

DJO, LLC

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

Recall #:

88721

Lot/product code:

Serial Numbers: 22753580

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

88651

Lot/product code:

All lots

Recalling firm:

Datascope Corp.

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

Recall #:

88664

Lot/product code:

All lots

Recalling firm:

Datascope Corp.

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

Recall #:

88664

Lot/product code:

All lots

Recalling firm:

Datascope Corp.

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

Recall #:

88651

Lot/product code:

All lots

Recalling firm:

Datascope Corp.