infant product Recalls

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

Boothwyn Pharmacy Fluorescein 2% Ophth 3 mL Recall for Subpotent Drug (High Risk)

Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (4 mL, 2.5 mg/mL)

Boston Scientific Neuromodulation Recall Affects 25,260 Vercise DBS Systems Over Wire Break Risk

Rite Aid Alcohol Prep Pads Recalled Over Subpotent Isopropyl Alcohol Levels (2025)

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

Walmart ReliOn Sterile Alcohol Swabs Recalled for Subpotent Isopropyl Alcohol (2025)

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

Medline Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol in 6669874 Units

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

H-E-B inControl Alcohol Pads Recalled for Subpotent Isopropyl Alcohol (2025)

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

CURAD Alcohol Prep Pads Recall for Subpotent Isopropyl Alcohol (2025)

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

Tandem Diabetes Care Recalling 19 Units of t:slim X2 Insulin Pump Over RTL App Defect (2025)

an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to incorrect therapy decisions and subsequent hypoglycemia or hyperglycemia.

North American Rescue JETT Medical Device Recall for Lower-Limb Occlusion Tool (2025)

Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.

CHETAK NEW YORK Deep Sprouted Mat 16 oz Recalled for Salmonella Risk 2025

Ford recalls 2025 Expedition air bags for passenger-side deployment risk

Ford Motor Company (Ford) is recalling certain 2025 Navigator and Expedition vehicles. The passenger side air bag may have been manufactured incorrectly, which can cause the air bag to deploy with excessive force during a crash.

BulkSupplements.com Inositol Recall Affects 1,001 Units Over Possible Staphylococcus Contamination (

Finished product possibly contaminated with pathogenic Staphylococcus aureus.

GM Recalls 2024-2025 Chevrolet Blazer EV for Parking Brake Wiring Harness Issue

General Motors, LLC (GM) is recalling certain 2024-2025 Chevrolet Blazer EV vehicles. The rear parking brake wiring harness may become damaged or corroded, resulting in unintended activation of the parking brake or loss of the parking brake function.

Beckman Coulter MicroScan Neg MIC 3J REF C54814 Recall for Missing Drug in Well 4/4 and Antibiotic D

Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics

Subaru 2025 Forester Recall for Loose Child Seat Anchor Bolts Affects Safety (HIGH Risk)

Subaru recalls 2025 Forester vehicles due to potentially loose child seat anchor bolts. Dealers will inspect and tighten bolts at no charge. Owner letters are expected August 15, 2025. Contact Subaru at 1-844-373-6614. Recall number WRC-25.

Quidel Dipstick Strep A Tests Recalled for Potential False Positives (Z-2545-2025)

Dipstick strep A test has potential for false positive results.

Sedecal SA SM-40HF-B-D-C Mobile X-ray System Recall for Cleaning Not Water-Resistant Risk (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.

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.