Safety Recall Directory
Browse and filter the latest official safety alerts globally.
UPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This i...
Contains statement does not declare Salmon
COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI cod...
Due to customer complaint regarding incorrect display box labeling.
CAREone, EXTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 750 mg, 96 chewable T...
Presence of foreign substance: small metallic particles in chewable tablets.
TopCare health, ULTRA STRENGTH, Antacid Tablets, CALCIUM CARBONATE 1000mg, 72 CH...
Presence of foreign substance: small metallic particles in chewable tablets.
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.
Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per...
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE ...
Contains statement does not declare pecan or walnut.
Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Via...
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewabl...
Presence of foreign substance: small metallic particles in chewable tablets.
UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer. This is Albertson's store-made...
Contains statement does not declare Almond.
GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable...
Presence of foreign substance: small metallic particles in chewable tablets.
Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2...
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used ...
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the followi...
The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis ...
Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY ...
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2....
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
UPC 25748400000 STICKY BUNS GOURMET WALNUT 4CT Th...
Contains statement does not declare Walnut
UPC 21843300000 READY MEALS TUNA SALAD & MUENSTER CHEESE SNACK PACK ...
Contains statement does not declare Tuna
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"...
Sterile wound dressing, lacks sterility assurance
Aligned Medical AMS16835 Fluids Kit RX
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL,...
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.