Recalls affecting Tennessee

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

Recall #:

87251

Lot/product code:

Batch Number: 342452 348027 351950 357125 364537 380155 380156 385417

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: 332506 338836 342573 344105 350523 361814 364756 366089 369339 379083

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: 333021 333022 338840 341489 343445 346886 351527 351528 351528 351528 351528 351528 351528 358459 358459 358459 358459 358459 358459 362405 363444 364766 364766 369197 369197 370268 377838 377838 379930 379930 379930 379930 379931 379931 385407

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: 333014 333016 338837 341887 343444 346882 351523 355020 361818 364757 367810 369360 370401 372233 379926

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: 329483 338820 344091 348578 353381 363435 364051 367788 372225 372226 379406

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: 328898 328899

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: 330512 330513 338827 340984 344095 350509 350510 352675 361797 364055 364747 367798 370387 372182 377185 378428

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: 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: 342453 348028 351951 357126 364538 370411 380157

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: 333154 338847 341490 347128 351533 359850 364536 367817 370409 378062 380154

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: 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: 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 #:

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 #:

87434

Lot/product code:

Catalog Number: HARH36 GTIN: 07613327346251 Lot Number: 12444050

Recalling firm:

Stryker Sustainability Solutions

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 #:

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 #:

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: 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

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

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

Recall #:

D-0304-2021

Lot/product code:

Lot #: 148992, Exp 5/31/2022

Recalling firm:

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

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

Recall #:

87331

Lot/product code:

Serial Numbers: 2258046 2863490

Recalling firm:

Stryker Communications

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

Recall #:

87274

Lot/product code:

Catalog Numbers HNM-31-150365 (lots 1017G, 1117B, 1217B, 0418C, 0518D, 0518H, 0618B, 0618D, 0818E, 1018J, 1018M, 1118J, 1218B, 1119B, 0420H, 0820H); HNM-31-150367 (lot 1117D); HNM-31-150368 (lot 1117D).

Recalling firm:

Bovie Medical Corporation