Recalls affecting South Dakota

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

Recall #:

80771

Lot/product code:

00868579000209.

Recalling firm:

Ortho Kinematics, Inc

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

Recall #:

77508

Lot/product code:

Lot No. 4123/MY33613, 4250/MY06614, 4279/MY06614, 4305/MY10814, 4331/MY13914, and 4331/MY25214

Recalling firm:

Myelotec, Inc.

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

Recall #:

76807

Lot/product code:

Product Codes: ASY00116 and ASY00281 Serial # All patients with Drivelines splice repair performed prior April 2015

Recalling firm:

Heartware

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

Recall #:

D-0691-2017

Lot/product code:

US lot 5GN767, expiration April 2017; lot 5GN773, expiration April 2017; lot 6GN215, expiration Sep 2017: INTERNATIONAL lot 5GR765, expiration March 2017; lot 5GK771, expiration April 2017; lot 5ED824, expiration April 2017; and lot 6ED117, expiration ***

Recalling firm:

Meridian Medical Technologies a Pfizer Company

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

Recall #:

D-0690-2017

Lot/product code:

US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017; lot 6GM088, exp. Oct 2017; lot 6GM087, exp. Oct 2017; lot 6GM198, exp. Oct 2017; lot 6GM081, exp. Sep 2017; lot 6GM091, exp. Oct 2017; lot 6GM199, exp. Oct 2017: INTERNATIONAL: lot 5FA665, exp. April 2017; lot 5GU763, exp. May 2017; lot 6FA293, exp. Oct 2017; lot 6FA292, exp. Oct 2017; lot 6GH294, exp. Oct 2017.

Recalling firm:

Meridian Medical Technologies a Pfizer Company

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

Recall #:

78036

Lot/product code:

Part No. 401AC (Lot No. 14K87246, 15M96863, 13E72645, 12D61386, 13D72302, 16B97593, 15C91286, 13B64377, 14J86547, 12B59416, 13A69334, 15K95972, 15A97196, 15E92377, 15F92378, 13L77336, 12D61023, 14G84704, 14K87499, 14F84193, 13L77335, 16B97594, 15C91419, 13B70167, 15C91448, 15E92375, 15K96046, 16A97197, 12B59529, 16B97798, 15K96125, 16B97595, 15L96777, 12D61829, 13D72644, 15A89998, 13F73449, 12M64134, 15L96745, 15D90215, 15H95035, 13F74403, 13L78489, 13L77336, 12H65961, 14G84878, 12F62179, 14J87014, 12B55182, 14F84444, 14J87081, 13L77336, 13L78489, 14F84400, 12J66632, 16A97380, 12M68130, 15E92376, 14L88737, 14L87904, 12K66633, 13H74994, 13H74995, 12B60056, 12C57285, 14H86266, 16A97592, 14J87164, 12D59168, 14M89765, 12A54328, 15A89854, 14F84634, 14G84624, 15M96829, 15K95896);    Part No. 402AC (Lot No. 13E73262, 15E92379, 12E57286, 12L68344, 15E93385, 12H65752, 12H65787, 15F92380, 12J65322, 15F92381, 12K67454, 15A89941, 15A89282, 13H75930, 12F55548, 12K67533, 13H75930, 12J66809, 12B59570, 15E92010, 12A50150, 14E83393);    Part No. 409AC (Lot No. 12C56215, 12B56215, 15C90920, 15K28358, 12C60069, 13B70035, 16B97312, 13A69520, 14E83602, 13E73264, 12L68584, 11M57610, 12F59571, 15B90832, 15E92560, 12K63370, 16B97614, 12L54648, 15D92011, 12M63372, 14H85773, 16B97615, 15M97109, 16B97805, 12M69229, 15A89939, 15A90196, 12F60692, 14L88520, 14L88519, 13A70145, 15E92382, 15A90466, 13E73450, 15F92383, 13D72925)

Recalling firm:

Measurement Specialties Inc

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

Recall #:

77198

Lot/product code:

Serial numbers: NBS101, NBS106, NBS140, NBS141, NBS145, NBS148, NBS155, NBS159, NBS163, NBS164, NBS166. NBS158 has been scrapped.

Recalling firm:

Nexstim PLC

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

Recall #:

77198

Lot/product code:

Serial numbers: NBS10391245N4, NBS11011250N4, NBS11071252N4, NBS11201252N4, NBS11451264N4, NBS11491268N4, NBS12051269N4, NBS12261274N4, NBS12341276N4, NBS12441278N4, NBS13341282N4, NBS13431283N4, NBS13451284N4, NBS13481286N4, NBS14011288N4, NBS14361295N5, NBS14481298N5, NBS14491299N5, NBS14511301N5, NBS15131302N5, Serial numbers: NBS10391245N4, NBS11011250N4, NBS11071252N4, NBS11451264N4, NBS11491268N4, NBS12051269N4, NBS12261274N4, NBS12341276N4, NBS12441278N4, NBS13341282N4, NBS13431283N4, NBS13451284N4, NBS14011288N4, NBS14481298N5, NBS14491299N5, NBS14511301N5, NBS15131302N5, NBS15271305N5, NBS15371307N5, NBS16031313N5 and NBS16221316N5. Additionally in Nexstim's warehouse (i.e. not distributed NBS 11201256N4, NBS 13481286N4, NBS 14361295N5 and NBS 16371318N5)

Recalling firm:

Nexstim PLC

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

Recall #:

D-0626-2017

Lot/product code:

Lot #: 6ZP9848, Exp 03/18; 6ZP0003, 6ZP9944, Exp 04/18.

Recalling firm:

GlaxoSmithKline, LLC

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

Recall #:

77102

Lot/product code:

73H1600207

Recalling firm:

Teleflex Medical

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

Recall #:

89765

Lot/product code:

4AM663, 4AM669, 4AR391, 4AR445, 4AR797, 4AR790, 4AR795

Recalling firm:

Craftmatic Industries, Inc.

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

Recall #:

89765

Lot/product code:

4AT056, 4AT061, 4AT063

Recalling firm:

Craftmatic Industries, Inc.

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

Recall #:

77025

Lot/product code:

All EP-Tracer -FSCA-identifier (2017-04-06)

Recalling firm:

CardioTek BV

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

Recall #:

D-0862-2017

Lot/product code:

Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02

Recalling firm:

Hospira Inc.

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

Recall #:

77121

Lot/product code:

Code: 131600, 131601, 131602, 131603, 131604, 131500, 131501, 131502, 131503, 131504 and 131506.

Recalling firm:

Molnlycke Health Care, Inc

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

Recall #:

F-2294-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2312-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2314-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2306-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2304-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2311-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2302-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2316-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2308-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2292-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC