IntegraDose Compounding Services LLC recalls fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719…
Lack of Assurance of Sterility: leaking bags
Read the official notice →- Date
- 2024-04-10
- Country
- United States
- Brand
- IntegraDose Compounding Services
- Product
- fentaNYL Citrate 2,500 mcg/50mL in Sterile Water, 50 mL CADD for Injection, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE,…
- Classification
- Class II
- Units
- Nationwide within the U.S
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More IntegraDose Compounding Services recalls
- 2026-06-24
US
- 2026-05-27
US
- 2025-10-22
US
IntegraDose Compounding Services LLC recalls Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719…
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
- 2024-02-21
US
IntegraDose Compounding Services LLC recalls Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx…
Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.
- 2024-01-31
US
- 2021-10-06
US
Other drugs & medical recalls in the United States
- 2024-04-10
US
SleepNet Corporation recalls Mojo 2 Full Face AAV Non Vented Mask, All Sizes
Update to contraindications and warning language due to CPAP masks containing magnets.
FDA · DeviceSleepNet CorporationWorldwide distribution - US Nationwide and the countries of AUSTRIA, BAHRAIN,…Official notice →US
SSM Health Care St. Louis DBA SSM St. Clare Health Center recalls Phenylephrine HCl, 1000 mcg/10 mL, 10 mL Total Volume per syringe, Intravenous, Rx Only,…
Lack of Assurance of Sterility: Firm did not perform process validation.
US
X-Gen Pharmaceuticals Inc. recalls Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After…
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg…
US
B. Braun Medical Inc recalls Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00
Lack of assurance of sterility: bags have the potential to leak..
US
Glenmark Pharmaceuticals Inc., USA recalls Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only,…
Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
- 2024-04-03
US
Boston Scientific Corporation recalls OptiCross Coronary Imaging Catheter, REF H749518080120
Certain batches of Opticross 40MHz Coronary Imaging Catheters manufactured using an incorrect voltage setting, which may have resulted in decreased image brightness.
FDA · DeviceBoston Scientific CorporationInternational distribution to the country of Japan.Official notice →