Recalls affecting Kansas

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

Recall #:

D-0256-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 08162016B (02/12/2017).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0322-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 05232016B (11/19/2016), 07272016C (11/30/2016), 07152016H (11/30/2016), 09152016B (12/31/2016), 11022016B (05/01/2017), 06082016B (11/30/2016), 08172016C (12/31/2016), 10202016C (02/28/2017).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0285-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07222016B (09/01/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0320-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 08022016F (12/08/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0251-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06092016B (0724/2016), 07212016C (09/04/2016), 09162016A (10/31/2016), 11012016A (12/16/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0315-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 05232016E (07/07/2016), 06092016C (07/17/2016), 05022016E (05/22/2016), 06232016D (08/04/2016), 06202016B (07/17/2016), 06152016E (07/17/2016), 06082016E (07/17/2016), 06022016C (07/17/2016), 07282016F (09/08/2016), 07262016G (09/04/2016), 07222016D (09/04/2016), 07192016D (09/01/2016), 07152016F (08/22/2016), 07082016C (08/22/2016), 08292016C (09/29/2016), 08052016C (09/16/2016), 08042016H (09/18/2016), 08022016E (09/16/2016), 09272016C (11/06/2016), 11012016B (12/09/2016), 05192016B (07/03/2016), 06132016F (07/17/2016), 06292016D (08/04/2016), 06222016E (08/04/2016), 06162016B (07/31/2016), 06132016C (07/17/2016), 06072016D (07/17/2016), 06012016D (07/16/2016), 07222016E (09/04/2016), 07202016A (09/01/2016), 07182016C (09/01/2016), 07132016B (08/22/2016), 07062016E (08/04/2016), 08092016F (09/18/2016), 08042016J (09/06/2016), 08032016D (09/16/2016), 09072016D (09/29/2016), 10132016C (11/24/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0281-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06162016B (07/17/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0319-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07112016B (08/22/2016), 09222016H (11/06/2016), 10252016F (12/09/2016), 09232016S (11/06/2016), 09072016E (09/29/2016), 11032016F (12/09/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0250-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07262016E (12/31/2016), 10262016E (02/28/2017).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0266-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07282016H (01/24/2017), 09282016E (03/27/2017)

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0253-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 09302016D (11/14/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0291-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06152016C (12/12/2016), 10242016C (04/22/2017).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

D-0246-2017

Lot/product code:

Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06012016A (11/28/2016), 07282016A (12/31/2016).

Recalling firm:

Tri-Coast Pharmacy

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

Recall #:

80981

Lot/product code:

Serial Numbers within U.S.A commerce - 1302002, 1302003, 1302005, 1302009, 1302011, 1402001, 1402002, 1402006, 1402007, 1402008, 1402009, 1402011, 1402012, 1402015, 1502001, 1502002, 1502004, 1502005, 1502006, 1502007, 1602001, 1602002, 1602003, 1602005, 1602006, 1602007 & 1602008   Serial Numbers Outside of U.S.A commerce - 1402005, 1402017, 1502009, 1502010, 1502011, 1302004, 1302006, 1302007, 1302008, 1302010, 1402003, 1402004, 1402010, 1402013, 1402014, 1402016, 1502008 & 1602004

Recalling firm:

Swissray Medical

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

Recall #:

79362

Lot/product code:

Model Number 6 ENT

Recalling firm:

Seiler Instr. & Mfg. Co. Inc.

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

Recall #:

76279

Lot/product code:

All lots of lenses sold between 10/31/2013 to 10/31/2016

Recalling firm:

The See Clear Company

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

Recall #:

80680

Lot/product code:

UDI: 00868579000209

Recalling firm:

Ortho Kinematics, Inc

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

Recall #:

76494

Lot/product code:

Batch number: 15486

Recalling firm:

Kiscomedica S.A.

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

Recall #:

D-0469-2017

Lot/product code:

Lot #'s: 437600, Exp 07/17; 447100, Exp 10/17

Recalling firm:

VistaPharm, Inc.

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

Recall #:

76600

Lot/product code:

HeartWare HVAD System Controller Product numbers: 1401US, 1401XX, 1403US, 1407XX, and 1400 with the serial Number(s) lower than CON300000 HeartWare HVAD DC Adapter Product number: 1435  .

Recalling firm:

Heartware

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

Recall #:

F-1695-2017

Lot/product code:

Lot Numbers: (a) Sell by Date: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017 (d) Best if used by: 02/28/2017 through 08/14/2017 (e) Best if used by: 02/28/2017 through 08/14/2017 (f) USE BY: 02/28/2017 through 08/14/2017 (g) Best if used by: 02/28/2017 through 08/14/2017 (h) Best if used by: 02/28/2017 through 08/14/2017 (i) Best if used by: 02/28/2017 through 08/14/2017 (j) Best if used by: 02/28/2017 through 08/14/2017 (k) Best if used by: 02/28/2017 through 08/14/2017

Recalling firm:

MDS Foods Inc

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

Recall #:

F-1706-2017

Lot/product code:

Lot Numbers: (a) Best if Used by: 3/28/2017 (b) Best if Used by: 3/28/2017 (c) Best if Used by: 004-17 (d) Best if Used by: 004-17

Recalling firm:

MDS Foods Inc

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

Recall #:

F-1698-2017

Lot/product code:

Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017

Recalling firm:

MDS Foods Inc

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

Recall #:

F-1710-2017

Lot/product code:

Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017

Recalling firm:

MDS Foods Inc

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

Recall #:

F-1702-2017

Lot/product code:

Lot Numbers: (a) Best if Used by: 3/28/2017, 4/25/2017, 5/26/2017, 7/3/2017 (b) Best if Used by: 4/18/2017 (c) Best if Used by: 4/22/2017 (d) Best if Used by: 018-17 (e) Best if Used by: 3/10/2017, 4/22/2017 (f) Best if Used by: 2/28/2017, 5/4/2017 (g) Best if Used by: 273-16 (h) Best if Used by: 004-17, 358-16 (i) Best if Used by: 320-16 (j) Best if Used by: 5/18/2017 (k) Best if Used by: 4/18/2017 (l) Best if used by: 02/28/2017 through 08/14/2017

Recalling firm:

MDS Foods Inc