Medicines & devicesClass II
Lupin Pharmaceuticals Inc. recalls Clobetasol Propionate Cream USP
Failed content uniformity specifications.
· FDA · Nationwide
Recalls
Safety recalls that rarely make the news, straight from the official U.S. agency records (FDA, USDA, CPSC, NHTSA). Every listing links to its official notice. We only copy what the record says.
Checked Nov 3, 10:23 AM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
1107 recalls
Medicines & devicesClass II
SUN PHARMACEUTICAL INDUSTRIES INC recalls Carbamazepine Tablets
CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing
· FDA · Nationwide
Medicines & devicesClass II
Shoolin Pharma Chem LLP recalls 5 products
CGMP Deviations:Noted during FDA inspection
· FDA · Nationwide
Medicines & devicesClass II
Beckman Coulter Mishima K.K. recalls Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96
Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError AlarmDB when launching the instrument software, using PC pre-instal
· FDA · Nationwide
Medicines & devicesClass II
Baxter Healthcare Corporation recalls Brand Name: VOLARA System Product Name: VOLARA
Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and testing confirmed devices meet specifications.
· FDA · Nationwide
FoodClass I
EURO FOODS GROUP USA NJ INC recalls Crown Farms Dried Suri Cut
The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
· FDA · MI, NJ, NY, VA
FoodClass I
Blank Slate Creamery Production recalls Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES
undeclared egg
· FDA · MI
FoodClass I
Ukrop's Homestyle Foods Recalls Spaghetti and Chicken Products Due to Possible Foreign Matter Contamination
High - Class I · Class I
· USDA FSIS · NC, VA, WV
Medicines & devicesClass I
Liebel-Flarsheim Company LLC recalls Optiray Imaging Bulk Package-350
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
· FDA · Nationwide
Medicines & devicesClass II
Jenavalve Technology Inc. recalls 3 products
Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.
· FDA · Nationwide
Medicines & devicesClass II
New York Embroidery Studio, Inc. recalls New York Embroidery Studio Trinity Non-Surgical Isolation Gown
Gowns do not consistently meet the minimum liquid-barrier performance required.
· FDA · Nationwide
Medicines & devicesClass II
GE Healthcare recalls 6 products
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record
· FDA · Nationwide
Medicines & devicesClass II
Philips North America recalls 2 products
Due to software malfunction, patient information system may freeze and become unresponsive.
· FDA · Nationwide
Medicines & devicesClass II
Bayer Medical Care, Inc. recalls MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System
Some devices may not have been properly sterilized due to a manufacturing sterilization issue.
· FDA · Nationwide
Medicines & devicesClass II
Maquet Cardiopulmonary Gmbh recalls 3 products
The packaging may not consistently maintain sterile barrier integrity.
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls 4 products
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
· FDA · Nationwide
Medicines & devicesClass II
WELL LEAD MEDICAL CO. LTD recalls SunMed Tracheal Tube
The 6Fr suction catheter could not pass through the samples smoothly.
· FDA · Nationwide
Medicines & devicesClass II
Johnson & Johnson Surgical Vision, Inc. recalls HEALON EndoCoat PRO
Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, withdraw cannula and reassess the insertion
· FDA · Nationwide
FoodPublic Health Alert
FSIS Issues Public Health Alert for Chicken Salad Product that May Be Contaminated with Listeria
Public Health Alert · Public Health Alert
· USDA FSIS · OR, WA
FoodClass II
Ukrop's Homestyle Foods LLC recalls 2 products
Foreign object: metal fragments
· FDA · KY, NC, VA
Medicines & devicesClass II
Heritage Pharmaceuticals Inc recalls CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
· FDA · Nationwide
Medicines & devicesClass II
Datex-Ohmeda, Inc. recalls 4 products
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling c
· FDA · Nationwide
Medicines & devicesClass II
GE Medical Systems Information Technologies Inc recalls Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04
Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.
· FDA · Nationwide
Medicines & devicesClass II
Howmedica Osteonics Corp. recalls 12 products
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increas
· FDA · Nationwide
Medicines & devicesClass I
Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove o
· FDA · 32 states
Household & products
15-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Enhomee-Direct
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety
· CPSC · Nationwide
Household & products
5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by KAIFAM
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety
· CPSC · Nationwide
Household & products
BenQ America Recalls GV31 Portable Projectors Due to Risk of Serious Injury or Death from Fire and Burn Hazards
The recalled projectors' lithium-ion battery can overheat, posing a risk of serious injury or death from fire and burn hazards.
· CPSC · Nationwide
Household & products
Galanz Americas Recalls Retro Refrigerators Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
The recalled refrigerators' internal electrical components can short circuit and ignite, posing a risk of serious injury or death from fire and burn hazards.
· CPSC · Nationwide
Household & products
Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
The cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion haz
· CPSC · Nationwide
Recall data comes from official U.S. government sources: openFDA (food, drugs, devices), USDA FSIS (meat, poultry, egg products), CPSC (consumer and children’s products) and NHTSA (vehicles, equipment, car seats). openFDA notes its data should not be relied on for medical decisions. Always confirm with the official notice. Check your vehicle by VIN at nhtsa.gov/recalls.