FDA Medical devices recall ·
See DocMan recall
- Recall number
- Z-0788-2025
- Date
- (initiated November 21, 2024)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 65310 units
- Hazard tags
- Sterility Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
See DocMan
Why was it recalled?
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
1) REF CDS930177C, UDI/DI 10889942810949 (EA) 40889942810940 (CS), Lot Numbers: 19BBO293, 19CBI818, 19EBC020, 19IBS311, 19JBP366, 19LBY043, 19VBE320, 20CBD448, 21ABE744, 21BBN653; 2) REF CDS982054V, UDI/DI 10193489552799 (EA) 40193489552790 (CS), Lot Numbers: 19BBJ530, 19CBL695, 19EBN805, 19EBZ133; 3) REF CDS982683X, UDI/DI 10198459064548 (EA) 40198459064549 (CS), Lot Numbers: 24IBH460; 4) REF CDS982719X, UDI/DI 10198459064531 (EA) 40198459064532 (CS), Lot Numbers: 24IBE288, 24JBB766, 24KBA129; 5) REF CDS983467J, UDI/DI 10195327561116 (EA) 40195327561117 (CS), Lot Numbers: 24ADA818, 24ADC216, 24BDA929, 24DDB447, 24EDA275, 24EDA751, 24GDB213, 24IDA327, 24IDB043, 24IDB372; 6) REF CDS983470C, UDI/DI 10889942730407 (EA) 40889942730408 (CS), Lot Numbers: 19ADC620, 19BDA241, 19CDA866, 19DDA314, 19DDD395, 19FDB295, 19GDA719, 19HDD614, 19JDB841, 19LDB812; 7) REF CDS983470I, UDI/DI 10195327561154 (EA) 40195327561155 (CS), Lot Numbers: 23LDA393, 24ADC171, 24DDA672, 24EDB254, 24FDC148, 24IDB368; 8) REF CDS983799D, UDI/DI 10193489592030 (EA) 40193489592031 (CS), Lot Numbers: 19FKB592, 19HKC268, 19IKA490, 19IKB968, 19JKA055, 19KKC040, 19LKB631, 20CKA736, 20HKB175, 21FLA865, 21ILA106, 21KLA781, 22ILA060, 22ILA292, 23HLA184; 9) REF CDS985212A, UDI/DI 10193489596335 (EA) 40193489596336 (CS), Lot Numbers: 19ABY900, 19FBT060, 19IBL327, 19PBA051; 10) REF CDS985212B, UDI/DI 10193489779820 (EA) 40193489779821 (CS), Lot Numbers: 19LBU107, 19VBH315, 20BBO078, 20CBW525, 20DBT438, 20GBH006, 20IBN419,
Distribution
Worldwide distribution - US Nationwide and the countries of UAE, and Canada.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0788-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.