54 recalls tagged with “back to school”.
B Braun Medical recalled its IV Administration Set used with Infusomat Space Large Volume Pumps and related models. The recall cites backflow of medication from secondary to primary IV containers and an occlusion that prevents priming. Hospitals and clinicians should stop using the device immediately and follow manufacturer recall instructions.
CA Botana International recalled 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 after CGMP deviations were identified. The recall covers tubes sold in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and contact the company for guidance.
Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser after detecting elevated benzene levels. The recall covers products associated with Lot # 58170A and Lot # 58172A distributed in CA and GA. Consumers should stop use and seek guidance from a healthcare provider.
BigTree Sales recalled its BT-GERMWAND-LRG-WHT handheld UV-C germicidal wand sold in the United States after FDA enforcement flagged unsafe UVC emissions. The device reaches the exposure limit for Risk Group 3 in about 2.2 minutes, creating a risk of skin and eye injuries. Stop using the device immediately and follow the recall instructions provided by the manufacturer.
Baxter Healthcare recalls 49,200 CONTINU-FLO IV Solution Sets distributed nationwide in the United States. IV sets may leak. Healthcare facilities and patients should stop using the device immediately and follow Baxter's recall instructions.
Baxter Healthcare Corporation recalled 958,351 CLEARLINK CONTINU-FLO IV sets due to a leak risk. The non-vented sets feature three Luer activated valves and a Backcheck Valve. Distribution covered nationwide in the United States. Healthcare providers and patients should stop using the device immediately and follow recall instructions on the recall notice.
Baxter Healthcare recalled 8,368 CLEARLINK SYSTEM CONTINU-FLO IV sets nationwide after reports the devices may leak. The non-vented sets include a 0.2-micron filter, three CLEARLINK luer activated valves and a backcheck valve, and measure 102 inches in length. Hospitals and clinicians should stop using these units immediately and follow Baxter's recall instructions.
B. Braun Medical Inc. recalled 16,228 3000 mL saline irrigation bags nationwide in the United States. The recall cites lack of assurance of sterility due to port misalignment, creating a potential for fluid leakage. Healthcare providers and patients should stop using the product immediately and contact the company for guidance.
Baker's Authority recalls 197 units of Everything Bagel Mix after undeclared sesame and other ingredients. The product label failed to list sesame and other ingredients. Consumers who bought the mix should not consume it and should seek a refund or replacement.
Monica Vinader recalls select 14k yellow gold mini heart bracelets, necklaces and stud earrings due to high cadmium levels. The recalled jewelry was manufactured in October and November 2024. Consumers should stop wearing the jewelry immediately and contact Monica Vinader for a replacement or refund.
Backyard Kids recalled KidKraft Farm to Table Play Kitchens in 2025 after one death was reported at multiple retailers. The hazard arises from hooks that hold toy accessories where clothing can snag during climbing or crawling through the back opening. Stop using the play kitchen immediately and contact Backyard Kids for free replacement hooks or repair.
Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.
DermaRite Industries’ DermaKleen antiseptic lotion soap is recalled nationwide after contamination with Burkholderia cepacia. The Class I recall covers 11,321 bag-in-box units sold nationwide. Consumers are urged to stop using the products and contact the company for guidance.
Volkswagen Group of America recalls 2024-2025 Atlas Cross Sport and Atlas vehicles for rearview camera distortion in reverse. The defect may reduce visibility behind the vehicle and increase crash risk. Dealers will update the camera control unit software free of charge. Owner letters mailed June 5, 2025. Contact VW customer service at 1-800-893-5298.