Recalls affecting North Carolina

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

Recall #:

87251

Lot/product code:

Batch Number: 330970 330971 338828 340985 344096 350511 350512 352676 355019 361799 364056 367799 369334 370389 372183 372184 378429 378430

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 342457 348032 351955 357129 364769 381292

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 332504 338834 344103 350521 353385 361808 364753 367807 370398 379081

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 345222 352337 357118 364543 372238 382115 386005

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 330973 330975 330976 338830 338831 344099 344100 350516 350517 356798 358456 361803 361804 364749 369336 370393 377188 379018 379542 379543 379544 380874

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 329484 338821 341497 344092 348579 353382 363436 367789 372223 372224 379407

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 333019 333020 338839 341491 346885 351526 354405 359842 359843 363443 364532 369362 370404 377837 379929 385416

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 329485 338822 341498 344093 348580 353383 363437 364053 369331 372220 379408

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 333017 333018 338838 346883 346884 351525 354404 358458 359841 364531 369361 370402 377835 377836 379927

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 345224 352339 357120 364544 370418 382117

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 345223 352338 357119 372239 382116

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 345225 352380 357121 359852 370419 382118

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 330510 330511 338826 344094 350507 355018 361793 361794 364054 372180 372181 377184 378427

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 333150 338842 341492 347125 351529 351530 358480 359845 364533 367814 369363 370406 377839 380043 380044 381527 381528 382443 382444 382445

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 342456 348031 351954 357128 364540 370414 381213 381525 383204

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 330972 330973 338829 344097 344098 350514 350515 352677 358455 361801 361802 364748 367803 369335 370391 370392 377187 379016 379539 379540 379541

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87251

Lot/product code:

Batch Number: 332500 338833 344102 350520 353384 361807 364751 364752 369338 377190 379080 380872

Recalling firm:

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

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

Recall #:

87221

Lot/product code:

Outer box GTIN: 08714729855934 Inner pouch GTIN: 08714729861263 Lot/Batch#: 25053639  Outer box GTIN: 08714729855903 Inner pouch GTIN: 08714729861294 Lot/Batch#: 24948407, 24670592, 24679619, 24676929, 24939628  Outer box GTIN: 08714729861300 Inner pouch GTIN: 087147298 61294 Lot/Batch#: 24770325, 24952552, 24665104  Outer box GTIN: 08714729861317 Inner pouch GTIN: 08714729861294 Lot/Batch#: 24679614, 25054403  Outer box GTIN: 08714729861348 Inner pouch GTIN: 08714729861324 Lot/Batch#: 24772995

Recalling firm:

Boston Scientific Corporation

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

Recall #:

87258

Lot/product code:

Lot Number L-008926-16037 Lot numbers L-008918-16048, and L-008918-16045  Lot numbers L-008936-16275, and L-008933-16078

Recalling firm:

ReNovo, Inc.

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

Recall #:

87221

Lot/product code:

Outer box GTIN: 08714729019251 Inner pouch GTIN: 08714729747680 Lot/Batch#: 24725319, 24782695,   Outer box GTIN: 08714729019312 Inner pouch GTIN: 08714729747833 Lot/Batch#: 24842597, 24812577,   Outer box GTIN: 08714729019336 Inner pouch GTIN: 08714729747857 Lot/Batch#: 24889757, 24719202, 24709536, 24773287,   Outer box GTIN: 08714729019350 Inner pouch GTIN: 08714729747871 Lot/Batch#: 24782693, 24732964, 24889755, 24780939,   Outer box GTIN: 08714729071068 Inner pouch GTIN: 08714729747970 Lot/Batch#: 24882357, 24782689, 24782687, 24729758,   Outer box GTIN: 08714729019411 Inner pouch GTIN:08714729747932 Lot/Batch#: 24961643  Outer box GTIN:08714729501640 Inner pouch GTIN: 08714729747932 Lot/Batch#: 24961645, 24989260, 24844193,   Outer box GTIN:08714729501657 Inner pouch GTIN:08714729747956 Lot/Batch#: 25010054,   Outer box GTIN:08714729019459 Inner pouch GTIN:08714729747994 Lot/Batch#: 25016793.

Recalling firm:

Boston Scientific Corporation

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

Recall #:

87281

Lot/product code:

Catalog Number: 612054, 613650, 614650, 672055, 673656, 673662, 674655, 674668, 674669, 716154, 762055, 763656, 763662, 765100, 765559, 772055, 773656, 773662, 775100, 775659, 776150

Recalling firm:

Cardinal Health 200, LLC

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

Recall #:

87221

Lot/product code:

Outer box GTIN: 08714729283904 Inner pouch GTIN: 08714729747598 Lot/Batch#: 24818278, 24906823, 25042455  Outer box GTIN: 08714729283928 Inner pouch GTIN: 08714729747611 Lot/Batch#: 24685766, 24817145, 24899710, 24739786, 25006735, 24861901  Outer box GTIN: 08714729158110 Inner pouch GTIN: 08714729748069 Lot/Batch#: 24685764, 24890051, 24824132  Outer box GTIN: 08714729268802 Inner pouch GTIN: 08714729748069 Lot/Batch#: 25023345  Outer box GTIN: 08714729158141 Inner pouch GTIN: 08714729748083 Lot/Batch#: 24699718, 24939626, 24861739  Outer box GTIN: 08714729268819 Inner pouch GTIN: 08714729748083 Lot/Batch#: 24824134, 25006729, 24709534  Outer box GTIN: 08714729501664 Inner pouch GTIN: 08714729748083 Lot/Batch#: 25023203, 24697822, 24739587, 24942292, 24909214, 24824136  Outer box GTIN: 08714729158158 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24856636, 24927642, 24699218  Outer box GTIN: 08714729268826 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24835709, 24818605, 25023343  Outer box GTIN: 08714729501671 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24909216, 24758832, 24872119, 24994171, 25048397, 2475126, 24929431, 24995438

Recalling firm:

Boston Scientific Corporation

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

Recall #:

87434

Lot/product code:

Catalog Number: HARH36 GTIN: 07613327346251 Lot Number: 12444050

Recalling firm:

Stryker Sustainability Solutions

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

Recall #:

D-0249-2021

Lot/product code:

Lot MET200601, 07/2022

Recalling firm:

Nostrum Laboratories Inc

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

D-0303-2021

Lot/product code:

a) Lot #: 148969, Exp 7/31/2022, b) Lot #: 148791, Exp 7/31/2022, c) Lot #: 148991, Exp 7/31/2022

Recalling firm:

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals