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Recalls in Delaware

Recalls sold in Delaware, including nationwide recalls, newest first.
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6 recalls

Zimmer Off-Axis Comprehensive Shoulder System Reamer Guides

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Moderate risk, FDA, Device defect

Chevrolet Express and GMC Savana Vehicles

The steering gear assembly may have a nut that was not properly tightened, which can cause loss of steering control and increase crash risk.

NHTSA, Steering defect

Rockford Fosgate Amplifier Kits

The amplifier kits have inadequate fuse protection that can increase the risk of a fire.

NHTSA, Electrical system defect

Ricon S-Series and K-Series Wheelchair Lifts

Wheelchair lifts may fail to stop, increasing injury risk.

NHTSA, Mobility equipment defect

5 recalls

Major Methylergonovine Maleate Tablets

Methylergonovine Maleate Tablets are subpotent.

Moderate risk, FDA, Wrong drug strength

Midwest Legacy Raw Beef Dog Food BLT & Bones

Midwest Legacy Raw Beef Dog Food BLT & Bones may be contaminated with Salmonella, Listeria, and E. coli O157:H7.

High risk, FDA, Salmonella

Ajanta Pharma Fenofibrate Capsules

Fenofibrate Capsules, USP 200 mg, have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

Philips Avalon Fetal Monitor

The Philips Avalon Fetal Monitor has incorrect speaker connector assembly that can cause loss of speaker output.

Moderate risk, FDA, Device defect

Forest River 2025-2026 NOBO, Ibex, and 2025-2027 RPOD Recreational Trailers

Recreational trailers have mislabeled 110V circuits that can cause electrical shock.

NHTSA, Electrical system defect

2 recalls

Airxcel MaxxAir N-Series Maxxfan Rooftop Ventilation Fans

MaxxAir N-Series Maxxfan rooftop ventilation fans have a printed circuit board that may overheat, posing a fire risk.

NHTSA, Vehicle equipment defect

Indian Motorcycle Company 2026 Chief Vintage Motorcycles

The 2026 Chief Vintage motorcycles have an incorrect rear rim width on the VIN label, which could lead to loss of control and a crash.

NHTSA, Vehicle equipment defect

17 recalls

Arizer Solo III Portable Electronic Vaporizers

Arizer Solo III portable vaporizers can explode or ignite, posing fire and burn hazards.

CPSC, Fire hazard

BABESIDE Doll and Stroller Toys

BABESIDE doll and stroller toys have small parts that can choke young children, posing a risk of serious injury or death.

CPSC, Choking hazard

GOPO TOYS Pull String Teething Toys

Pull string teething toys have silicone strings that are too small and long, posing a choking hazard.

CPSC, Choking hazard

Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller

The Joolz Aer2 Car Seat Adapters can fail to attach properly, allowing the car seat to fall and posing a risk of serious injury.

CPSC, Fall hazard

CooCooBaby Baby Loungers

CooCooBaby Baby Loungers have unsafe sides and padding, posing suffocation and fall hazards.

CPSC, Suffocation hazard

Michley Children's Pajamas

Michley children's pajamas violate flammability standards, posing a risk of serious burn injuries or death.

CPSC, Burn hazard

Veseacky Pajama Sets

Veseacky Pajama Sets violate children's sleepwear safety standards, posing a burn hazard that can cause serious injury or death.

CPSC, Burn hazard

Keystone Topical Anesthetic Gels

Topical anesthetic gels may have defective containers with incomplete seals.

Moderate risk, FDA, Packaging defect

HeartMate 3 Left Ventricular Assist System Kits, System Controller, and Backup Battery

Due to 11 volt Backup Battery failures.

Moderate risk, FDA, Device defect

STAAR ICL Calculation Software

The STAAR ICL Calculation Software has a coding issue that affects the implant orientation diagram printout.

Moderate risk, FDA, Software defect

Inspire Respiratory Sensing and Stimulation Lead

The Inspire Respiratory Sensing Lead has an incorrect Use By Date, which may lead to unplanned revision surgery.

Moderate risk, FDA, Labeling error

Merit Medical Systems Splashwire Hydrophilic Guide Wire

The Splashwire Hydrophilic Guide Wire has unsealed portions of pouches.

Moderate risk, FDA, Packaging defect

Piaggio 2026 Liberty 50 and Liberty 150 motorcycles

The 2026 Liberty 50 and Liberty 150 motorcycles have a headlight that may fail, reducing visibility and increasing crash risk.

NHTSA, Electrical system defect

2026 Toyota BZ, Lexus RZ, and Subaru Solterra Battery Electric Vehicles

The electronic control unit may experience a fault, resulting in a loss of drive power.

NHTSA, Electrical system defect

Farber Specialty 2025 45 MCXCR and 2025-2026 HX620 SBA 6X4 Emergency Vehicles

The touchscreen display may fail, preventing activation of emergency lights and equipment, increasing crash and injury risk.

NHTSA, Vehicle equipment defect

Cadillac Vistiq

The third-row power seatback may fail to reverse when activated, and a person may be trapped, increasing injury risk.

NHTSA, Seat defect

Beta Bionics iLet Bionic Pancreas

This can lead to hyperglycemia.

Moderate risk, FDA, Software defect

5 recalls

Endo Buprenorphine HCl Injection

Buprenorphine HCl injection has crystallization identified as Buprenorphine free base.

Moderate risk, FDA, Quality problem

Medline Urethral Catheters and Procedure Kits

Medline urethral catheters and kits may have surface irregularities or connector issues.

Moderate risk, FDA, Quality testing problem

GE HealthCare Giraffe OmniBed Devices

The Giraffe OmniBed has a potential issue with the canopy soffit that could cause patient injury.

Moderate risk, FDA, Device defect

ConMed AirSeal Access Ports and Obturators

ConMed AirSeal Access Port and Obturator may cause overpressure alerts.

Moderate risk, FDA, Device defect

Mito Red Light Super Mobile

The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.

Moderate risk, FDA, Device defect

3 recalls

Smith & Nephew Trigen Proximal Straight Humeral Nail

The humeral nail is missing distal holes and may lead to revision surgery if implanted.

Moderate risk, FDA, Manufacturing problem

Arrogantf Spa Drain Covers

Spa drain covers pose entrapment and drowning hazards due to violating safety standards.

CPSC, Entrapment hazard

Storyteller Overland GXV Hilt Vehicles

GXV Hilt vehicles have a secondary alternator pulley that may fail, causing loss of power brakes and power steering.

NHTSA, Electrical system defect

6 recalls

Ajanta Pharma Aripiprazole Tablets

Aripiprazole Tablets USP are mislabeled, containing Voriconazole Tablets instead.

Moderate risk, FDA, Labeling error

Medtronic O-Arm O2 Imaging System

The O-arm O2 Imaging System may show image artifacts due to a detector panel firmware anomaly.

Moderate risk, FDA, Software defect

ALYON and HarmonyAIR A-Series Surgical Lighting System

The surgical lighting system has light intensity control buttons that may detach.

Moderate risk, FDA, Device defect

HarmonyAIR A-Series Surgical Lighting System

The HarmonyAIR A-Series Surgical Lighting System has paint that may chip or peel on its light heads.

Moderate risk, FDA, Device defect

Forest River XLR Toy Hauler Recreational Trailers

XLR Toy Hauler trailers have an incorrect weight rating label, which may lead to overloading and a crash risk.

NHTSA, Vehicle equipment defect

Wabash Van Trailers

Wabash van trailers have improperly tightened bumper tube bolts, reducing rear impact protection and increasing injury risk in a crash.

NHTSA, Vehicle structure defect

3 recalls

Nara Organics Whole Milk Organic Infant Formula

Product may be contaminated with C. botulinum (botulism).

High risk, FDA, Botulism

Arrow International Vascular Access and Catheterization Kits

Paracentesis kits contain lidocaine, bupivacaine.

High risk, FDA, Sterility problem

Waymo 5th Generation Automated Driving Systems

Waymo 5th Generation Automated Driving Systems may allow a vehicle to enter a closed freeway construction zone and drive at speed, increasing crash risk.

NHTSA, Electrical system defect

14 recalls

Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments

Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

Inventia Healthcare Chlorthalidone Tablets

Chlorthalidone Tablets fail dissolution specifications.

Moderate risk, FDA, Drug dissolving problem

Sandoz Focalin XR Extended-Release Capsules

Labeling: Incorrect or Missing Lot and/or Exp Date.

Low risk, FDA, Labeling error

Glenmark Alyacen 7/7/7 and Norethindrone and Ethinyl Estradiol Tablets

Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.

Moderate risk, FDA, Drug impurity

IntegraDose Compounding Services Vasopressin Syringes

Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride is subpotent.

Moderate risk, FDA, Wrong drug strength