outdoor Recalls
134 recalls tagged with “outdoor”.
Sun Pharmaceutical Radiopharmaceutical Kit Recall: 1,870 Kits Recalled for OOS Dissolution Issue
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
PHILIPS Allura Xper FD10/10 Recall Tied to BIOS Battery Depletion

Zydus Lifesciences Succinylcholine Chloride Injection Recall Active for Unknown Impurity Degradation
Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.
Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected
Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

Philips Ingenuity CT Brazil 728325 CT System Recalled for 3 Units in 2025
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
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.

Fieldsheer Recalls Heated Socks MWMS07 MWWS07 MWMS05 for Burn Hazard (2025)

Deale International Recalls Altafit AF28 Smartwatches Sold by HSN for Fire Hazard
Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Recall: 85,950 Units (2025)
Maquet Vasoview Hemopro 3 EVH System Recall Affects 98 Units, 16 Complaints of Out-of-Box Failures
Maquet Cardiovascular recalled 98 Vasoview Hemopro 3 EVH systems nationwide across FL, IL, MD and TX after 16 out-of-box failure complaints. No serious injuries were reported. The failures occurred during limited launch before clinical use.
Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec
Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.
Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)
Due to incorrect/lack of Unique Device Identifier (UDI) codes.

Transpro US Recalls Electric Scooters for Unauthorized Battery Labels, Fire Risk

Winston Products HydroTech 5/8-Inch Expandable Burst-Proof Hose Recall 2025

iMirror Recalls Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter (2025)
This recall involves the Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter for indoor and outdoor use. There is a rectangular silver sticker displaying model number BZ-001 on the back of the electric mosquito swatter handle.
Hyundai IONIQ 5 2025 Recall for High Voltage Battery Bus Bar Tightening Short Circuits (2025)
Hyundai Motor America (Hyundai) is recalling certain 2025 IONIQ 5 vehicles. The high voltage battery system may contain an improperly tightened bus bar, which can cause a short-circuit.