Recalls affecting Kentucky

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

Recall #:

71130

Lot/product code:

Pack 670-057

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 693-223

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 888-2359, 888-2531, 888-2351

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 888-2533

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 693-196, 693-188, 693-166, 693-112, 888-2583

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 888-2606

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 888-2493

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 693-210, 693-054, 693-219, 888-2479, 888-2499

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 888-2489

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 670-056, 681-014

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 682-126

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 681-012, 888-2385

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71130

Lot/product code:

Pack 888-2604

Recalling firm:

Stradis Healthcare, LLC.

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

Recall #:

71242

Lot/product code:

Serial #: ALL HeartWare HVAD systems currently in use.

Recalling firm:

HeartWare Inc

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

Recall #:

71240

Lot/product code:

Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205. Serial #: ALL HeartWare HVAD systems currently in use.

Recalling firm:

HeartWare Inc

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

Recall #:

71099

Lot/product code:

Catalog #: ASY00116: HVAD Pump Driveline Splice Kit Lot #'s 532770, 567949, 480786, 483769, 490692, 539664, and 598189 and Catalog #: ASY00281: HVAD Pump Driveline Splicekit; Large OD Sheath Lot #'s 654090, 672401, 678800, 690423, 833963, 873159, and 880816

Recalling firm:

HeartWare Inc

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

Recall #:

71241

Lot/product code:

Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101, 1102, 1104, 1104JP and 1205. Serial #: ALL HeartWare HVAD systems currently in use.

Recalling firm:

HeartWare Inc

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

Recall #:

71164

Lot/product code:

Serial #: ALL HeartWare HVAD systems currently in use.

Recalling firm:

HeartWare Inc

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

Recall #:

71239

Lot/product code:

Serial #: ALL HeartWare HVAD systems currently in use.

Recalling firm:

HeartWare Inc

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

Recall #:

71160

Lot/product code:

Affected lots begin with: 14DMLB, 14EMLB, 14HMLB, 14JMLB, 14KMLB, 14LMBL, 14NMLB, 14PMLB, and 14SMLB.

Recalling firm:

Fresenius Medical Care Holdings, Inc.

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

Recall #:

71649

Lot/product code:

Delta, Delta Element, Delta Plus, DPO-4000-XX-U-EN-EN-PM-SP12, DPO-6000-XX-U-EN-EN-AP-SP10.

Recalling firm:

Olympus Scientific Solutions Americas

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

Recall #:

D-1242-2015

Lot/product code:

31075DK, 31076DK, EXP01JUL2015; 32345DK, 32368DK, EXP 01AUG2015; 33152DK, EXP 01SEP2015; 34538DK, EXP 01OCT2015; 37227DK, EXP 01JAN2016, 41525DK, 42255DK, EXP 01MAY2016; 46042DK, 46045DK, 46048DK, 46304DK, 46305DK, 46432DK, 46433DK, EXP 01OCT2016 AND NOVAPLUS LOT 31074DK, EXP 01JUL2015

Recalling firm:

Hospira Inc.

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

Recall #:

D-1241-2015

Lot/product code:

31077DK, 31078DK, 31338DK, 31339DK, 31340DK, EXP 01JUL2015; 32068DK, 32069DK, EXP 01AUG2915; 33270DK, EXP 01SEP2015; 34084DK, 34085DK, 34161DK, 34162DK, 34298DK, 34299DK, 34300DK, EXP 01OCT2015; 35011DK, 35081DK, 35082DK, 35116DK, EXP 01NOV2015; 38139DK, 38140DK, 36144DK, EXP 01FEB2016; 39256DK, 39257DK, EXP 01MAR2016; 42210DK, 42227DK, EXP01JUN2016; 43017DK, 43116DK, 43117DK, 43292DK, 43293DK, EXP 01JUL2016; 45034DK, 45035DK, 45118DK, 45120DK, EXP 01SEP2016; 46310DK, 46311DK, EXP 01OCT2016 AND NOVAPLUS LOTS 32106DK, 32220DK, 32221DK, EXP 01AUG2015; 33235DK, 33236DK, EXP 01SEP2015; 34163DK, 34164DK, EXP 01OCT2015; 39263DK, 39264DK, EXP 01MAR2016

Recalling firm:

Hospira Inc.

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

Recall #:

D-1165-2016

Lot/product code:

Lot 1220062085, Exp. 09/16

Recalling firm:

XTREME Z DISTRIBUTORS INC

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

Recall #:

D-0664-2016

Lot/product code:

Lot # 000815004400; Exp 12/17

Recalling firm:

Life and More LLC