Reported Dec 4, 2024 · Ongoing
MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF…
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- MEDLINE
- procedure kits labeled as follows
1) ECHOSTIM BLOCK SETREF DYNJRA9043S2) ULTRASOUND BLOCK PREP TRAYREF PAIN1622A
- Lot codes and dates
- Codes1) DYNJRA9043S, UDI/DI 10193489888287(each) 40193489888288(case)
- Lot Numbers23CBE390, 23CBO216, 23EBM309, 23EBP979, 23EBS281, 23GBV099, 23HBG915, 23IBG610, 23IBG611, 23JBQ712, 23KBC341; 2) PAIN1622A, UDI/DI 10193489891690 (each) 40193489891691 (case)
- Lot Numbers
21ELA82121GLA61521KLA30822ALA60822CLA68122ELB08822FLB07522GLA54322KLA01923BLA33323DLA46623HLA896
- Amount recalled
- 3396 units
This recall covers 12 products
The agency filed one notice per product. You are reading one of them; the other 11 are below.
Where it was sold
- Nationwide
Why it was recalled
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
This product could cause temporary or reversible health problems — stop using it.
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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