Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
IntegraDose Compounding Services LLC recalled 853 bags of Oxytocin 30 Units/500 mL on September 16, 2025. Testing revealed these IV bags contain no oxytocin, posing serious health risks. The recall affects products distributed nationwide in the USA.
American Health Packaging recalled 360 cartons of Carbamazepine Extended-Release Tablets on September 15, 2025. The tablets fail to meet dissolution specifications, posing a risk to patients. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Alcon Research LLC recalled 28,323 CONSTELLATION ULTRAVIT and HYPERVIT devices on September 15, 2025, due to a high hazard risk. The recall affects products distributed worldwide, including multiple states in the U.S. and several countries.
Graviti Pharmaceuticals recalled 46,512 bottles of Bupropion Hydrochloride Extended-Release Tablets on September 15, 2025. The recall stems from failed tablet specifications that could affect safety and efficacy. The product was distributed to pharmacies nationwide.
FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray tube support on September 15, 2025, due to a potential shaft failure. The broken shaft could render protective components ineffective, posing a high risk during operation. Healthcare providers and patients must stop using the device immediately.
Private Label Skin Care recalled 125 units of ARTISAN OF SKIN Benzoyl Peroxide 10% on September 12, 2025. Elevated benzene levels prompted the recall in California and Georgia. Consumers should stop using the product immediately and seek guidance.
Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser on September 12, 2025. The recall follows the discovery of elevated benzene levels in the product. This contamination poses a high health risk to consumers in California and Georgia.
Private Label Skin Care recalled its edunn clarity BP Treatment Cleanser on September 12, 2025. Elevated benzene levels prompted the recall after post-consumer awareness. The product was distributed in California and Georgia.
Private Label Skin Care recalled its 7 oz Acne Treatment on September 12, 2025. Elevated levels of benzene prompted the recall, classified as Class II. The affected product was distributed in California and Georgia only.
Private Label Skin Care recalled Benzaderm BPO Cleanser 10% on September 12, 2025. Elevated benzene levels prompted the recall affecting consumers in California and Georgia. No injuries have been reported.
Private Label Skin Care recalled its Micronized BPO Gel Cleanser 10% on September 12, 2025. Elevated benzene levels prompted the recall in California and Georgia. Consumers must stop using the product immediately and seek guidance from healthcare providers.
GE HealthCare recalled 64 units of the Elscint Model 4XX gamma camera on September 12, 2025. The recall affects systems that lack adequate support during transport, risking detector falls. If the detectors fall, they can cause serious injuries to patients and healthcare providers.
GE HealthCare recalled 15 nuclear medicine gamma cameras on September 12, 2025. The recall affects systems that may have been relocated without proper support, risking detector falls. This poses a significant danger of life-threatening injuries to patients and healthcare providers.
GE HealthCare recalled 1,386 nuclear medicine gamma cameras on September 12, 2025. Certain models may have been relocated without proper support, risking detector integrity. This could lead to life-threatening injuries from falls.
GE HealthCare recalled 11 Cardial nuclear medicine gamma cameras on September 12, 2025. The recall follows concerns over inadequate detector support potentially leading to life-threatening falls. The affected systems were transported without proper safeguards, compromising safety.
GE HealthCare recalled a dual-head nuclear medicine gamma camera on September 12, 2025, after identifying a risk of detector falls. One unit is affected, posing a high risk of life-threatening injury. Users must stop using the device immediately and follow manufacturer instructions.
Shanghai United Imaging Healthcare Co., Ltd. recalled 11 units of its uCT 760 MD Computed Tomography X-ray System on September 12, 2025. The recall addresses a serious hazard where third-party outer covers can become trapped between the patient table and gantry, leading to mechanical interference. Healthcare providers and patients must stop using the device immediately and follow recall directives
UIH Technologies recalled 95 units of its uMI 550 Positron Emission Tomography and Computed Tomography System on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, posing a mechanical interference risk. Patients and healthcare providers must stop using the device immediately.
Diagnostica Stago recalled 12,740 D-Dimer testing devices on September 12, 2025. The recall follows a risk of underestimating D-Dimer levels in patients. Healthcare providers and patients should stop using the device immediately.
UIH Technologies recalled 8 units of its uCT 530 MD X-ray system on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, causing mechanical interference. Healthcare providers and patients must stop using the device immediately.