In the agency's Nov 11, 2026 enforcement report · Ongoing
Cardinal Health Presource PBDS kits, Containing BD Alaris Pump Infusion Sets used with BD Alaris Pump Module Model…
Cardinal Health 200, LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337
Is this the product you have?
35 of 35 products
| Model / number | Product as published |
|---|---|
MA1JV8300C | KIT,LABOR KIT |
MA1JV8300B | KIT,LABOR KIT |
PL42VDATM3 | KIT, VAGINAL DELIVERY |
MA1JV83001 | KIT,LABOR KIT |
PL42VDATM2 | KIT, VAGINAL DELIVERY |
PL42VDATMN | KIT, VAGINAL DELIVERY |
MA1JV8300A | KIT,LABOR KIT |
PL42VDATMB | KIT, VAGINAL DELIVERY |
PBJVAD00S | LABOR, KIT |
PL41OTHS4 | KIT,LABOR |
PL42VDATMA | KIT, VAGINAL DELIVERY |
PL41OTHSV | KIT,LABOR |
PL42VDATML | KIT, VAGINAL DELIVERY |
PL42VDATMK | KIT, VAGINAL DELIVERY |
PBJVAD00X | KIT,LABOR KIT |
PL42VDATMJ | KIT, VAGINAL DELIVERY |
PBJVAD00W | LABOR KIT, ,KIT |
PBJVAD00U | LABOR KIT, ,KIT |
PL42VDATMH | KIT, VAGINAL DELIVERY |
PL42VDATMG | KIT, VAGINAL DELIVERY |
- Lot codes and dates
229 of 229 products
Products covered by this recall Model / number Barcodes Product as published 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #500060 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #500060 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #500060 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #500060 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #519838 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #519838 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #541166 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #541166 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #541166 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #541166 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #561757 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #561757 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #561757 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #582974 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #605722 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #605722 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #605722 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #605722 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #630532 1088748848314650887488483144CATALOG #MA1JV8300C, (ea) 50887488483144 (cs), LOT #630532 - Amount recalled
- 47707 kits
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Why it was recalled
Stop using this product now
Kits contain infusion sets which were recalled for performance issues.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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