elderly product Recalls

Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier (UDI) in 206 Units

The device does not bear a unique device identifier.

Max Mobility Permobil MX2+ SpeedControl Dial Recalled for 15,834 Units in 2025

Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.

Max Mobility/Permobil Recalls 25,389 MX2+ SpeedControl Dial Units (2025)

Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.

Max Mobility/Permobil Recalls 8,413 Smart Drive MX2+ SpeedControl Dials (2025)

Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall — 200 Units (2025)

The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Convenience kits labeled as sterile have not gone through the sterilization process.

Hi-Tech Pharmaceuticals Quercetin Dietary Supplement Recalled for Unapproved Drug Claims and Misbrnd

Unapproved Drug Claims and Misbranded.

SeaSpine Orthopedics Recalled 74 Reef TA Inserter Instruments for Reef Interbody System (2025)

Boston Scientific NephroMax Kit Recall Covers 458 Units Over Foreign Material Migration Risk

Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)

Waldemar Link Recall Reaches 8 Units of LinkSymphoKnee Tibial Components Over Uncoated Screws (2025)

Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.

Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Due to incorrect/lack of Unique Device Identifier (UDI) codes.

Taizhou Kangping Medical 3.85 Million Cartons of BZK Antiseptic Towelettes Recalled for Sterility LQ

Lack of Assurance of Sterility.

Middlefield Original Cheese Cooperative Pepper Jack Cheese Recalled for Listeria Contamination (2025

Potential contamination with Listeria monocytogenes

DJO Surgical AltiVate Reverse Glenoid Tray Recall Affects 439 Kits Nationwide (2025)

DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.

Walmart Recalls Ozark Trail 64 oz Water Bottles for Lid Ejection Hazard (2025)

Boothwyn Pharmacy Semaglutide 2.5 mg/mL 2 mL Vials Recalled for Subpotent Drug (HIGH)

Sedecal SM-40HF-B-D-C 40KW Mobile X-ray System Recalled for Cleaning Water-Resistance Issue (2025)

Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.