Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling a 0.9% Sodium Chloride Injection due to lack of assurance of sterility. This injectable medication may not be sterile, which could …
Fresenius Kabi USA, LLC
Recalls This Week
Every US government recall in one place: food, vehicles, consumer products, drugs, medical devices, and meat and poultry, rewritten in plain English and updated daily.
Updated Jun 4, 2026 · 1007 recalls tracked
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling 0.9% Sodium Chloride Injection due to lack of assurance of sterility. This injectable medication may be contaminated, which could …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling certain 0.9% Sodium Chloride Injection vials because the manufacturer cannot guarantee they are sterile. Using a non-sterile …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi USA is recalling 0.9% Sodium Chloride Injection 500 mL single-dose bags because the manufacturer cannot confirm the product is sterile. Sterile …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling 0.45% Sodium Chloride Injection in 250 mL bags because the company cannot guarantee the product is sterile. Non-sterile injectable …
Fresenius Kabi USA, LLC
Arjo Tenor Patient Lift Recall
Certain Arjo Tenor mobile patient lifts may have a defective internal component in the actuator that could suddenly lose its ability to hold the load, causing …
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
LSL Healthcare Wound Closure Tray Recall
LSL Healthcare Wound Closure Tray Model 7554 contains alcohol prep pads that were not properly sterilized. Non-sterile materials used during wound closure can …
LSL Healthcare Inc.
Payless Compounders Semaglutide Injectable Recall
Semaglutide-Glycine-Cyanocobalamin Injectable vials from Payless Compounders have not been verified as sterile and may be contaminated. Using a non-sterile …
PAYLESS COMPOUNDERS, LLC
2027 Telluride, 2026 K4 Seat Belt Recall
Certain 2027 Kia Tellurides and 2026 Kia K4 vehicles have rear seat belt anchor buckles that may not latch properly, risking occupant injury in a crash.
Kia America, Inc.
2027 Kia Telluride and 2026 Kia K4 Recall
The rear center seat belt anchor buckle on 2026 Kia K4 and the third-row center seat belt anchor buckle on 2027 Kia Telluride may fail to latch properly, …
Kia America, Inc.
Forever 21 Kids Mickey Mouse Pajama Pants Recall
Forever 21 Kids Disney Mickey Mouse Pajama Pants with black stripes have been recalled because they fail mandatory flammability standards for children's …
Forever 21 Kids Disney Mickey Mouse Pajama Pants
Tomum Minoxidil Hair Serum Spray Recall
Tomum Minoxidil Hair Growth Treatment spray bottles (100 mL) were recalled because their packaging is not child-resistant, as required by law. If a young child …
Tomum Hair Regrowth Treatment with Minoxidil for Men and Women Spray Bottles
HALO Magic Sleepsuit Recall: Choking Hazard
HALO Dream has recalled its Magic Sleepsuit because the zipper head can detach from the garment, creating a choking hazard for infants. Three specific batch …
HALO Magic Sleepsuits
Cubimana Island Storm 3-in-1 Building Set Recall
Cubimana Island Storm 3-in-1 Building Sets (model HG1004) have been recalled because the LED light piece contains button cell batteries that children can easily …
Cubimana Island Storm 3 In 1 Building Sets with LED Lights
Cook Medical Arterial Pressure Monitoring Tray Recall
Cook Medical's Arterial Pressure Monitoring Trays have been recalled because some units were labeled with expiration dates that are longer than their actual …
Cook Incorporated
Apotex Brimonidine/Timolol Eye Drop Recall
Apotex Corp. is recalling Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution because sterility cannot be assured. Use of a non-sterile eye drop can cause …
Apotex Corp.
Chevrolet Silverado 3500 Fuel Pump Recall
The rear fuel pump in certain 2025 to 2026 Chevrolet Silverado 3500 and GMC Sierra 3500 trucks may fail to deliver adequate fuel to the front tank, causing the …
General Motors, LLC
Angiodynamics Soft-Vu Catheter Recall
Angiodynamics' Soft-Vu Angiographic Catheter (Kumpe, non-braided) has a manufacturing defect that may block the guidewire from passing through the catheter hub. …
Angiodynamics, Inc.
Rising Pharma Temozolomide 5mg Recall
Rising Pharmaceuticals is recalling Temozolomide Capsules 5mg due to impurities found during stability testing. The capsules may contain unwanted chemical …
Rising Pharma Holding, Inc.
Ajinomoto Tai Pei Shrimp Fried Rice Recall
Ajinomoto Tai Pei Shrimp Fried Rice packages may contain small pieces of glass (1 to 3 cm long, 2 to 4 mm wide). Do not eat this product if you have it.
Ajinomoto Foods North America Inc.
Ajinomoto Ling Ling Fried Rice Recall
Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable contains glass fragments 1 to 3 cm long that could cause serious injury if ingested. The …
Ajinomoto Foods North America Inc.
Ajinomoto Gyoza Dumplings Recall
Ajinomoto Vegetable Gyoza Dumplings may contain pieces of glass (1 to 3 cm long). Do not eat the product if you have purchased it; glass fragments can cause …
Ajinomoto Foods North America Inc.
Ajinomoto Green Gyoza Dumplings Recall
Ajinomoto Green Gyoza Vegetable & Edamame Dumplings (12ct) are being recalled due to glass fragments (1 to 3 cm long) found in the product. Eating glass can …
Ajinomoto Foods North America Inc.
Farmhouse Fresh Midnight Clearing Lotion Recall
FarmHouse Fresh Midnight Clearing Night Lotion (2.5% benzoyl peroxide acne treatment) has been recalled due to benzene contamination. Benzene is a known …
Owen Biosciences Inc.
Artificial Tears Eye Drops Recall
Artificial Tears Sterile Lubricant Eye Drops sold under multiple store brands are being recalled because the manufacturer cannot guarantee they remain sterile. …
K.C. Pharmaceuticals, Inc
Philips ALLURA Xper FD20 Biplane Recall
The Philips ALLURA Xper FD20 Biplane X-ray system may fail to initiate imaging or produce only intermittent X-ray exposure when using the wired foot switch, …
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Ajinomoto Foods North America, Inc. Expands Recall for Chick
Ajinomoto Foods North America; Ajinomoto Toyo Frozen Noodle, Inc.; Ajinomoto Foods North America
AccuVu Angiographic Catheter Recall
AccuVu Angiographic Catheters with certain catalog and product numbers contain a manufacturing defect that may prevent a guidewire from passing through the …
Angiodynamics, Inc.
Ford F-250 F-350 Driveshaft Recall
The driveshaft on certain 2025 to 2026 Ford F-250 SD and F-350 SD trucks may separate due to a faulty friction weld, causing sudden loss of drive power and …
Ford Motor Company
2026 Ford E-450 Backup Alarm Recall
The backup alarm on certain 2026 and 2027 Ford E-350 and E-450 vehicles may fail to sound when reversing, increasing the risk of hitting a pedestrian or another …
Ford Motor Company
Get free recall alerts
One email when something you own gets recalled. No spam. Always free.
Free forever. Unsubscribe anytime. We never sell your data.