
FDA•MODERATE
Medline Red Rubber Latex Urethral Catheters
Medline recalls Red Rubber Latex Urethral Catheters (REF DYND13508–DYND13522, DYND13614/16) over surface, connector, and diameter defects.
34 products
Medline recalls Red Rubber Latex Urethral Catheters (REF DYND13508–DYND13522, DYND13614/16) over surface, connector, and diameter defects.
34 products
GE HealthCare recalls Giraffe OmniBed incubator/warmer over canopy soffit fastener risk that could injure patients.
3 products
ConMed recalls AirSeal 5 mm Access Port (iASB5-150) over overpressure alert risk.
11 productsStaar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.
2 products
Arrogantf spa drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.

Great Value Hawaiian Roll 4pk recalled over oily substance on food-contact packaging; product never reached store shelves.

Accriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control, level 2, due to incorrect performance range labeling.

Storyteller is recalling 2024-2026 GXV Hilt vehicles due to an alternator pulley failure that may cause a loss of power brakes and steering.

Ajanta Pharma is recalling Aripiprazole 30 mg tablets due to a mix-up with Voriconazole 50 mg tablets.

Medtronic is recalling the O-arm O2 Imaging System due to a firmware anomaly that may cause image artifacts during clinical use.

HarmonyAIR A-Series surgical lights recalled: intensity buttons may detach.
2 products
Steris is recalling HarmonyAIR A-Series Surgical Lighting Systems due to a risk of paint delamination on the light heads.

Forest River is recalling 2023-2024 XLR Toy Hauler trailers due to an incorrect GVWR that may lead to vehicle overloading and crash risk.

Wabash is recalling 2027 van trailers due to improperly tightened rear impact guard bolts that may fail to meet federal safety standards.
