Lower riskMedical device recall · FDA · Published October 27, 2021
Medline EVLP Kit Recalled: Expired NaCl Bag Risk
Medline recalls EVLP Convenience Kit with expired NaCl 250mL bag (lot 19HBE998) due to potential contamination. Affected kits may have expired saline solution.
NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.
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Contact the company
📍Recalling firmMedline Industries Inc3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer
Medline is recalling their EVLP Convenience Kit because the NaCl 250mL bag inside expired in April 2:2020, while the kit itself was still within its expiration date. Using this expired saline could lead to contamination risks if the kit is used for medical purposes. Read more at govinfonow.com/recall/61624-medline-evlp-kit-recalled-expired-nacl-bag-risk.
“Medline EVLP Kit Recalled: Expired NaCl Bag Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61624-medline-evlp-kit-recalled-expired-nacl-bag-risk. Based on FDA recall #Z-0358-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0358-2022%22&limit=1).
The FDA announced on 2021-10-27 that Medline Industries Inc is recalling the EVLP Convenience Pack/Kit. The hazard involves an expired NaCl 250 mL Bag Inj within the kit.
How to tell if you have it
EVLP Convenience Pack/Kit
Model #: DYNJ901205C
Lot #: 19HBE998
GTIN (01)40889942580607
UPC 40889942580607
The hazard
The recall involves NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.
Context
GovInfoNow's records show Medline Industries Inc has 48 other recalls on record since 2015-09-25. Other recent recalls of similar products include Medline Chest Tube Kit Recalled (2022-07-21), Medline Hand Sanitizer Foam Recall (2021-11-08), and Medline Stopcocks Recall (2021-08-06). Other recent recalls of similar products include Medline Convenience Kits Recalled Due to Potential Contamination (2026-07-10), Medline Convenience Kits Recall: Contaminated Components Risk (2026-07-10), and Medline convenience kits recalled due to potentially contaminated components (2026-07-10).
How to tell if you have this one
Check for model number DYNJ901205C and lot number 19HBE998 on the kit. The kit was sold with an expiration date of January 31, 2021.
Brand
Medline
Product
EVLP Convenience Pack/Kit
Category
Medical device
FDA recall event · 5 products
All 5 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
US Nationwide distribution.
Recall number
Product, codes & lots
Quantity
Z-0358-2022
EVLP Convenience Pack/Kit; Model #: DYNJ901205C Lot #: 19HBE998 UDI: GTIN (01)40889942580607 EXP (17)2021-01-31 LOT (10)19HBE998
28
Z-0359-2022
Neuro Convenience Kit; Model #: DYNJ905194 Lot #: 19HBK497 UDI: GTIN (01)40889942837466 EXP (17)2021-04-30 LOT (10)19HBK497
30
Z-0360-2022
Major Vascular CDS Convenience Kit; Model #: CDS981543D Lot #: 19HBK745 UDI: GTIN (01)4088277523976 EXP (17)2021-07-31 LOT (10)19HBK745
15
Z-0361-2022
Venous Access Pack-LF Convenience Kit; Model #: DYNJ36725B Lot #: 19UBB149 UDI: GTIN (01)40889942389163 EXP (17)2021-07-31 LOT (10)19UBB149
15
Z-0362-2022
Bedside PICC CDS Convenience Kit; Model #: CDS984642 Lot #: 19JBB553 UDI: GTIN (01)40884389882825 EXP (17)2021-09-30 LOT (10)19JBB553
1
Based on the official FDA remedy
What to do — step by step
Check Kit Expiration
Verify the model number DYNJ901205C and lot number 19HBE998 on the kit's label.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0358-2022 (October 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0358-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.