Medline Kits, trays, and packs labeled as follows: a) BREAST PACK, REF DYNJ56344B; b) SEPTOPLASTY PACK WRO-LF, RE
Summary
The FDA issued a Class I for Medline Kits, trays, and packs labeled as follows: a) BREAST PACK, REF DYNJ5 by MEDLINE INDUSTRIES, LP - Northfield. Reason: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Ch.
Details
Source
Device Recall
External ID
Z-1109-2024
Action Date
2024-03-06
Status
Ongoing
Category
device
Product Description
Medline Kits, trays, and packs labeled as follows: a) BREAST PACK, REF DYNJ56344B; b) SEPTOPLASTY PACK WRO-LF, REF DYNJ62803
Lot/Code Info: a) REF DYNJ56344B, UDI/DI 40889942612322 (case), 10889942612321 (unit), Lot Numbers: 22CLA043, 22HLA191, 22ILA180, 23BLA030, 23BLB019, 23ELA630; b) REF DYNJ62803, UDI/DI 40193489688994 (case), 10193489688993 (unit), Lot Numbers: 22GBS133, 23GBF930
Quantity Affected: 139 units
Reason for Recall
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Distribution
Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-15
Company
Northfield, IL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 205 device recalls issued in the same week, part of 413 device-related FDA actions this month.
MEDLINE INDUSTRIES, LP - Northfield has 822 FDA actions in our database, including 822 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MEDLINE INDUSTRIES, LP - Northfield) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MEDLINE INDUSTRIES, LP - Northfield have FDA actions?
MEDLINE INDUSTRIES, LP - Northfield has 822 FDA actions in our database, including 822 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1109-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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