Class II · Moderate risk
Acetaminophen Injection 1000 mg/100 mL
Discoloration
National Drug Code
Is NDC 36000-0306-60 recalled?
Acetaminophen · 40 BAG in 1 CARTON (36000-306-60) / 100 mL in 1 BAG
Yes — this exact package was recalled
2 FDA recalls name the code 36000-0306-60 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Acetaminophen
- Strength
- ACETAMINOPHEN 10 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Baxter Healthcare Corporation
- Type
- Human Prescription Drug
- Product code
- 36000-0306
Recalls naming this package
Class II · Moderate risk
Acetaminophen Injection
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 36000-0002 See recall 3
- 36000-0048 See recall 3
- 36000-0003 See recall 2
- 36000-0046 See recall 2
- 36000-0047 See recall 2
- 36000-0001 See recall 1
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