Health & Personal Care
HIGH
FDA DRUG
Glenmark Theophylline Extended-Release 400mg Recall Expanded for Failed Dissolution Tests (2025)
Glenmark Pharmaceuticals Inc.
Failed Dissolution
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DEVICE
Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.
Baxter Healthcare
Baxter Healthcare
Health & Personal Care
HIGH
FDA DRUG
Quallent Pharmaceuticals Health LLC Recall Expands for Duloxetine Delayed-Release Capsules Over Imp-
CGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.
DULOXETINE
CGMP deviations:
Health & Personal Care
HIGH
FDA DEVICE
PHILIPS IntelliSpace Cardiovascular Software 8.0.0.4 Recall Affects 4 Units Nationwide
Software issue that results in the display of outdated information.
Philips Medical Systems Nederland B.V.
Software issue
Health & Personal Care
HIGH
FDA DEVICE
Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
Schiller
Vital sign
Health & Personal Care
HIGH
FDA DEVICE
Medline Industries Recalls 22 Sterile Convenience Kits DYNJ0382730O, DYNJ61038B (2025)
Convenience kits labeled as sterile have not gone through the sterilization process.
Medline Industries
Convenience kits
Health & Personal Care
HIGH
FDA DEVICE
Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)
Convenience kits labeled as sterile have not gone through the sterilization process.
Medline Industries
Convenience kits
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol 3.125 mg Recall for Nitrosamine Impurity Affects 44,328 Bottles (2025)
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Glenmark Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol 25 mg Recall for Nitrosamine Impurity Affects 4,800 Bottles (2025)
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Glenmark Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol Tablets Recalled Over Nitrosamine Impurity
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Glenmark Pharmaceuticals Inc.
CGMP Deviations:
CRITICAL
CPSC
Séfralls Minoxidil Hair Generation Serum Recalled for Child Poisoning Risk (2025)
This recall involves Séfralls Hair Generation Serum. The hair serum comes in an amber dropper bottle with a white and gold dropper and a white, black and gold label. "Séfralls" and "Minoxidil" are printed on the label located on the front of the bottle.
Séfralls
The hair
HIGH
CPSC
Monica Vinader Recalls 14k Yellow Gold Mini Heart Jewelry Over Cadmium Levels (2025)
Monica Vinader
The jewelry
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals iFORCE Joint Help Recall 85,950 Units for Unapproved Drug Claims (2025)
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA DEVICE
Maquet Vasoview Hemopro 3 EVH System Recall Affects 98 Units, 16 Complaints of Out-of-Box Failures
Maquet Cardiovascular recalled 98 Vasoview Hemopro 3 EVH systems nationwide across FL, IL, MD and TX after 16 out-of-box failure complaints. No serious injuries were reported. The failures occurred during limited launch before clinical use.
Maquet Cardiovascular
On August
Health & Personal Care
HIGH
FDA DEVICE
Olympus ViziShot 2FLEX Biopsy Device Recalled for Deformed Tips in 103,731 Units
Potential for undetected, deformed a-traumatic tips.
Olympus Corporation of the Americas
Potential for
Health & Personal Care
HIGH
FDA DEVICE
SeaSpine Orthopedics Recalled 74 Reef TA Inserter Instruments for Reef Interbody System (2025)
SeaSpine Orthopedics
Inserter, used
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals Adderex XR Recall 85,950 Units for Unapproved Claims (2025)
Unapproved Drug Claims and Misbranded.
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals Top Secret Nutrition Uric Control Recalled 85,950 Units in 2025 for Unproved
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals Slimaglutide 85,950-Unit Recall for Unapproved Drug Claims (2025)
Unapproved Drug Claims and Misbranded.
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals Dietary Supplement LG Sciences Battle Hardener Platinum Series Recall for Un
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Recall: 85,950 Units (2025)
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals Formutech Nutrition Joint Formula Recalled for Unapproved Drug Claims (2025)
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA FOOD
Hi-Tech Pharmaceuticals Beta Sitosterol 715mg Recalled for Unapproved Claims (2025)
Unapproved Drug Claims and Misbranded.
Hi-Tech Pharmaceuticals
Unapproved Drug
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol 12.5 mg Tablets Recalled for NNCI Impurity Exceeding FDA Limit (2025)
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
Glenmark Pharmaceuticals Inc.
CGMP Deviations:
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