Vermont recalls

Medline is recalling specific lots of its blood culture kits because the BD ChloraPrep Triple Swabsticks inside may have damaged or open packaging seals. This could allow the applicators to dry out or become contaminated before use. The affected lots are 25EBU508 and 25EBE330.

Medline is recalling specific lots of suture removal kits that contain BD ChloraPrep Triple Swabsticks with potentially open or compromised packaging seals. An open seal on the applicators could allow contamination of the sterile product before use. No injuries have been reported.

Medline is recalling two medical convenience kits that contain BD ChloraPrep Triple Swabsticks with potentially open or compromised packaging seals. The affected kits are the POWERGLIDE DRESSING CHANGE KIT (SKU DYNDH1576, Lot 25EBP737) and CENTRAL LINE TRAY W/ CHLRP SWB (SKU RWM-DC57KC, Lot 25EBE082). An open seal could allow the sterile applicator to become contaminated.

Medline Industries is recalling 11 different medical kits that contain BD ChloraPrep Triple Swabsticks with potentially compromised packaging seals. The affected applicators may have open or broken seals, which could affect the sterility of the product. No injuries have been reported so far.

Medline is recalling eight types of medical convenience kits that contain BD ChloraPrep Triple Swabsticks with potentially opened or compromised seals. The affected kits are used in hospitals and medical settings for procedures involving central lines and ports. No injuries have been reported.

Medline Industries is recalling specific lots of Pediatric Cath Securement Kits (SKU DYNDC3108) because the BD ChloraPrep Triple Swabsticks inside may have open or compromised packaging seals. An open seal could allow the applicators to dry out or become contaminated before use.

Medline Industries is recalling specific lots of adult catheter securement kits (SKU DYNDC3109) because the BD ChloraPrep Triple Swabstick applicators inside may have broken seals on their packaging. This could allow the sterile applicator to become contaminated.

Medline Industries recalled specific lots of its Anesthesia Artline Pack kits because the BD ChloraPrep Triple Swabsticks inside may have open or compromised seals on the applicator packaging. An open seal could allow the sterilizing solution to dry out or become contaminated before use. No injuries have been reported.

Medline Industries is recalling certain lots of reprocessed Siemens ACUSON AcuNav ultrasound catheters because they may contain small particles of leftover material from reprocessing. If used, these particles could cause inflammation, infection, or blood clots that may lead to serious complications including stroke or pulmonary embolism.

Certain lots of reprocessed Biosense Webster SOUNDSTAR eco diagnostic ultrasound catheters may contain small particles of leftover material from manufacturing. If used, these particles could cause blood clots, infection, or other serious complications including stroke or lung embolism.

Medline Industries is recalling certain lots of reprocessed ViewFlex Xtra ICE Catheters (9F x 90cm) because they may contain small particles of leftover material inside the device. If used, these particles could trigger inflammation, infection, blood clots, or other serious complications.

Certain lots of reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters distributed by Medline may contain small particles of leftover material from reprocessing. If used in patients, these particles could cause blood clots, infection, or inflammatory reactions that may lead to serious complications including stroke or blood clots in the lungs or legs.

Medline Industries is recalling certain lots of reprocessed Livewire Steerable Electrophysiology Catheters because they may contain small particles of residual material left after reprocessing. If used, these particles could cause serious complications including infection, blood clots, or emboli.

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Medline Industries is recalling certain reprocessed Webster CS Catheters because they may contain small particles of leftover material from cleaning. If used, these particles could trigger inflammation, infection, blood clots, or serious complications like stroke or lung clots.

Philips has recalled three Spectral CT 7500 CT scanner systems because fasteners that secure the rotor inside the gantry may not have been tightened to the correct specification. If multiple fasteners are loose, rotor parts could become unsecured or displaced during operation. No parts have been expelled or injuries reported so far.

Philips has recalled certain Spectral CT imaging systems because fasteners that hold the rotor in place inside the gantry may not be properly tightened. If multiple fasteners are loose, rotor parts could potentially become displaced or expelled during operation. No injuries or equipment failures have been reported so far.

Philips has identified that fasteners holding the rotor in place inside certain IQon Spectral CT scanners may not be properly tightened. While no equipment failures or injuries have been reported, loose fasteners could theoretically cause rotor parts to become unsecured during operation.

Philips has recalled certain Brilliance iCT CT scanners because fasteners that secure the rotor inside the gantry may not be tightened to the correct specification. If multiple fasteners are loose, rotor parts could potentially become displaced or expelled during scanning. No injuries or incidents have been reported.

Hologic's Brevera Breast Biopsy System disposable 9 gauge needles may contain tiny particles that could be deposited into breast tissue during a biopsy procedure. This affects approximately 681,870 units distributed nationwide. No injuries have been reported so far.

Medline Industries intubation kits (SKU DYNJAA245B, lots 25IBC172 and 25HBJ413) may contain an 8 Fr suction catheter instead of the correct 14 Fr size. The smaller catheter can block the airway during intubation, potentially causing severe breathing problems or failure that requires emergency intervention.

Some Medline 14 Fr Suction Catheter Kits (SKU DYND40972) may contain a smaller 8 Fr catheter instead of the correct 14 Fr size. Using the wrong size catheter can partially or completely block the airway, leading to low oxygen levels and breathing failure that may require emergency treatment.

McKesson's UDENYCA (pegfilgrastim-cbqv) injection was stored at room temperature instead of in the refrigerator, which may have reduced its effectiveness. This affected 116 cartons from Lot 2199821 with specific serial numbers. The FDA classified this as a Class I recall.

Meitheal Pharmaceuticals is recalling Cetrorelix Acetate 0.25 mg injection kits because some contain missing or duplicated needles in the delivery system. This affects lot Q4E0112A with an expiration date of April 30, 2027. The defect could prevent proper injection or cause unsafe handling.

American Health Packaging is recalling certain oxycodone hydrochloride 5 mg tablets because the blister card seals are defective or missing. This allows tablets to fall out of their compartments. The recall affects 31,676 packages distributed nationwide with specific lot numbers and expiration dates.

Fresenius Kabi Compounding has recalled vancomycin HCl 2-gram doses mixed in sodium chloride solution due to concerns that sterility cannot be assured. The affected lots were distributed nationwide. This is a serious issue because non-sterile injectables can cause life-threatening infections.

Fresenius Kabi Compounding issued a recall of vancomycin HCl 1.5 grams in 500 mL sodium chloride solution due to lack of assured sterility. The affected lot (C274-000049628, expiring May 3, 2026) was distributed nationwide to healthcare facilities. No injuries have been reported.

Fresenius Kabi Compounding has recalled multiple lots of thiamine HCl 500 mg injection because the manufacturer cannot confirm the product is sterile. This injectable medication was distributed nationwide. The recall affects 10,548 bags with expiration dates between February and May 2026.

Fresenius Kabi Compounding has recalled five specific lots of ketamine HCl injection (10 mg per mL) distributed nationwide because the manufacturer cannot confirm the product remains sterile. The affected lots were produced between February and April 2026.

Fresenius Kabi Compounding has recalled acyclovir sodium 200 mg IV injection bags because the manufacturer cannot guarantee the product is sterile. The affected bags were produced by Fagron Sterile Services and have lot number C274-000049124 with an expiration date of February 28, 2026. No infections or injuries have been reported so far.