FDA Device recall Z-0167-2020

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL

FDA Device
Class II
terminated
Published 2019-10-30

On 2019-10-30 the FDA classified a Class II recall of EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL by Baxter Healthcare, citing potential ability to leak once used for compounding.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0167-2020
Classification	Class II
Status	terminated
Initiated	2019-09-18
Published	2019-10-30
Last updated	2026-09-13 11:55 UTC
Company	Baxter Healthcare
Distribution	US

Product

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2. H938738, 500mL; 3. H938739, 1000mL; 4. H938740, 2000mL; 5. H938741, 3000mL Product Usage: The EXACTAMIX Empty EVA bags are used as the destination container in compounding of large-volume sterile solutions for further administration to a single patient. The empty bags are used at pharmacies and compounding centers by pharmacists and pharmacy technicians to compound multi-ingredient solutions, as prescribed by a physician.

Reason

Potential ability to leak once used for compounding.

Identifiers

code_info	1. UDI Number: 00085412477213, Lot Numbers (60060391, 60061809, 60061816, 60061819, 60063137, 60063138, 60063141, 60063… 1. UDI Number: 00085412477213, Lot Numbers (60060391, 60061809, 60061816, 60061819, 60063137, 60063138, 60063141, 60063142, 60063143, 60063146, 60063147, 60063148, 60064545, 60064546, 60064547, 60064548, 60064549, 60064551, 60064552, 60064553, 60064554, 60066253, 60066254, 60066255, 60066256, 60066257, 60066258, 60068559, 60070835, 60070836, 60070837, 60074866, 60074955, 60074956, 60074959, 60075125, 60075170, 60080371, 60080372, 60080373, 60080374, 60080375, 60080376, 60081617, 60081618, 60081621, 60081622, 60081649, 60081650, 60081655, 60082887, 60083516, 60083519, 60084461, 60084462, 60084465, 60084466, 60084471, 60084472, 60084475, 60085739, 60085740, 60085741, 60085742, 60085743, 60085744, 60085745, 60086979, 60086980, 60086981, 60086982, 60086985, 60086986, 60088180, 60088181, 60088182, 60088183, 60088185, 60088186, 60089784, 60089785, 60089786, 60089787, 60089788, 60089789, 60091137, 60091138, 60091139, 60091140, 60091141, 60091142, 60092384, 60092407, 60092408, 60092409, 600924

code_info

1. UDI Number: 00085412477213, Lot Numbers (60060391, 60061809, 60061816, 60061819, 60063137, 60063138, 60063141, 60063…

1. UDI Number: 00085412477213, Lot Numbers (60060391, 60061809, 60061816, 60061819, 60063137, 60063138, 60063141, 60063142, 60063143, 60063146, 60063147, 60063148, 60064545, 60064546, 60064547, 60064548, 60064549, 60064551, 60064552, 60064553, 60064554, 60066253, 60066254, 60066255, 60066256, 60066257, 60066258, 60068559, 60070835, 60070836, 60070837, 60074866, 60074955, 60074956, 60074959, 60075125, 60075170, 60080371, 60080372, 60080373, 60080374, 60080375, 60080376, 60081617, 60081618, 60081621, 60081622, 60081649, 60081650, 60081655, 60082887, 60083516, 60083519, 60084461, 60084462, 60084465, 60084466, 60084471, 60084472, 60084475, 60085739, 60085740, 60085741, 60085742, 60085743, 60085744, 60085745, 60086979, 60086980, 60086981, 60086982, 60086985, 60086986, 60088180, 60088181, 60088182, 60088183, 60088185, 60088186, 60089784, 60089785, 60089786, 60089787, 60089788, 60089789, 60091137, 60091138, 60091139, 60091140, 60091141, 60091142, 60092384, 60092407, 60092408, 60092409, 600924

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0167-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.