FDA
Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured b… Recalled: Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
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Searching CPSC consumer products, FDA food & drug enforcement reports, and USDA meat & poultry recalls — sorted newest first.
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1,498 recalls found — page 6 of 63.
- FDA
Le Chef Bakery branded Mini Italian Pastry Assortment; 2.5 lbs/cs; (40 pieces/cs); packag… Recalled: undeclared colors (yellow#5)
undeclared colors (yellow#5)
- FDA
Chlorthalidone Tablets, USP, 25 mg, [100 or 1000] Tablets pr bottle, Rx only, Manufacture… Recalled: Failed Dissolution Specifications
Failed Dissolution Specifications
- CPSC
Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by Gudook Outdoor Sports
The recalled helmets violate the mandatory safety standard for?bicycle helmets?because the helmets do not comply with the impact attenuation and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- CPSC
Crenlux Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Eicong
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to swimmers and bathers.
- CPSC
Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions
The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows?and infant support cushions?because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.
- CPSC
Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin
The recalled drain covers violate the entrapment protection standards of the?Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to swimmers and bathers.
- CPSC
SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury
The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious injury if the elevator is called to another floor.
- CPSC
Tiny Land Children's Play Tents Recalled Due to Risk of Injury from Irritation to Skin and Eyes
The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation.
- CPSC
TOMY Recalls Boon NURSH 8 oz Reusable Baby Bottles Due to Choking Hazard; Sold at Walmart
The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children.
- CPSC
Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard
The recalled heater's fan blade can detach from the motor shaft, which can cause the fan to slow or stop, leading to overheating and melting of the enclosure and internal parts. Melted internal parts can ignite and breach the enclosure if the thermal cut off or fuse does not timely activate, posing a fire hazard.
- CPSC
Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury from Fire and Burn Hazards
The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium?ion battery's metal casing, causing the battery to rapidly overheat, posing a risk of serious injury or property damage from fire and burn hazards.
- FDA
prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC 70748… Recalled: Presence of Foreign Substance
Presence of Foreign Substance
- FDA
Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Lt… Recalled: Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg…
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
- FDA
Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oak… Recalled: Presence of Foreign Substance.
Presence of Foreign Substance.
- FDA
Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99)… Recalled: Presence of Foreign Substance.
Presence of Foreign Substance.
- FDA
Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One… Recalled: CGMP Deviations
CGMP Deviations
- FDA
Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pi… Recalled: sub potency
sub potency
- FDA
Sensipar (cinacalcet) Tablets, 90mg, 30-count bottles, Rx Only, Distributed by: Amge, One… Recalled: CGMP Deviations
CGMP Deviations
- FDA
Sensipar (cinacalcet) Tablets, 30mg, 30-count bottles, Rx Only, Distributed by: Amge, One… Recalled: CGMP Deviations
CGMP Deviations
- FDA
Gas-X Extra Strength, SIMETHICONE 125 mg/ANTIGAS, packaged in a) 120 SoftGels (UPC 3 0067… Recalled: Chemical Contamination: contamination with a diluted propylene glycol-based coolant from…
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.
- FDA
Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748… Recalled: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim…
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
- FDA
Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactur… Recalled: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim…
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
- FDA
MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein… Recalled: Potential physical contamination: dark spot was noticed on the bottom of container.
Potential physical contamination: dark spot was noticed on the bottom of container.