Delaware recalls

Datascope Corp. is updating the instruction manual for Cardiosave Hybrid devices to correct references in the Vibration and Shock Table to ensure alignment with applicable standards. This is a documentation correction that affects multiple device models.

Zimmer Surgical Inc. is recalling certain Dermatome AN surgical devices (Model 88710100) because the thickness control bar may be misaligned. This could affect the device's ability to cut skin grafts to the correct thickness during surgery. No injuries have been reported.

Zimmer Surgical Inc. is recalling certain Zimmer Air Dermatome surgical devices because the thickness control bar may be misaligned. This could affect how the device operates during skin grafting procedures. No injuries have been reported so far.

Medline Industries' sterile Kelly forceps (5.5 inch, Item DYNJ04048) may have packaging seals that don't hold properly. If the seal fails, the sterile barrier is broken, which could allow bacteria or other germs to contaminate the instrument and increase infection risk if used.

Medline Industries sterile surgical scissors (5.5", Item DYND04000, Lot 2023102590) may have weak packaging seals that could break during storage or handling. If the sterile packaging fails, the scissors could become contaminated and increase infection risk if used in surgery or medical procedures.

Mindray's BeneVision Distributed Monitoring System (DMS) workstations with specific hardware and audio driver configurations may experience audio playback failure or screen freezing during operation. This can affect the usability of the central monitoring system in clinical settings. About 906 units are affected worldwide.

GE Healthcare has recalled certain Power Management Boards in Carestation 600 and 700 Series anesthesia systems. If AC power is lost or unplugged, these systems may unexpectedly shut down instead of switching to battery backup, causing temporary disruption of ventilation and medication delivery. After restart, the system will not return to its previous settings.

GE Healthcare has recalled certain Carestation 750 anesthesia systems that may unexpectedly shut down if AC power is lost or unplugged. When this happens, the system will not automatically switch to battery backup and will reboot, which can temporarily disrupt ventilation and medication delivery. After rebooting, the system does not return to its previous settings.

GE Healthcare's Carestation anesthesia systems (600 and 700 Series) may unexpectedly shut down if AC power is lost or unplugged. When this happens, the system does not automatically switch to battery backup and will restart instead. During the restart, ventilation and anesthetic gas delivery may briefly stop, and the system will not return to previous ventilation settings after reboot.

Taro Pharmaceuticals is recalling specific lots of Ciclopirox Shampoo 1% because the product failed quality tests for impurities and degradation at the 18-month mark. The affected lots expire January 31, 2026. No injuries have been reported.

Preferred Pharmaceuticals is recalling ondansetron ODT 4mg tablets because the blister pack containers are not fully sealed, which can cause tablets to fall out. The manufacturer Glenmark Pharmaceuticals notified Preferred Pharmaceuticals of the sealing defect. This affects specific lot numbers distributed nationwide.

Somerset Therapeutics is recalling cisatracurium besylate injection (a muscle relaxant used during surgery) because stability testing found the drug strength fell below the required standard. Lot A250043 with expiration date 06/30/2026 is affected. The company has not reported any injuries.

Somerset Therapeutics is recalling cisatracurium besylate injection (200mg/20mL vials, Lot #A250020, expiration 06/30/2026) because stability testing found the drug's strength fell below required standards. This means the medication may not work as intended during medical procedures.

Somerset Therapeutics is recalling specific lots of cisatracurium besylate injection because testing found the drug contains less active ingredient than labeled. The affected vials may not work as intended during medical procedures. No injuries have been reported.

Golden State Medical Supply's baclofen 10 mg tablets in 1,000-count bottles (Lot GS065762) may contain foreign tablets or capsules mixed in. This affects 2,472 bottles distributed nationwide. No injuries have been reported.

OraVerse (phentolamine mesylate) injection cartridges in one lot have been found with cracks or breaks in the container. Affected cartons contain 10 cartridges each and were distributed nationwide. No injuries have been reported.

Novocol Pharmaceutical is recalling one lot of Carbocaine 3% mepivacaine injection because some cartridges in affected cartons are cracked or broken. Cracked containers can allow contamination or leakage of the medication. No injuries have been reported.

Benco Dental is recalling Mepivacaine HCI 3% injection cartridges (lot D05159H, expires 07-31-2027) because some cartridges may be cracked or broken. A defective container could allow the medication to leak or become contaminated. No injuries have been reported.

Novocol Pharmaceutical's Mepivacaine HCI 3% injection cartridges may have cracked or broken containers. This defect affects one lot (D05159G) distributed nationwide. The cracked cartridges could compromise the integrity of the medication.

Novocol Polocaine 3% dental anesthetic cartridges in one specific lot may have cracked or broken containers. This defect could compromise the sterility and safety of the medication. No injuries have been reported.

Novocol Pharmaceutical's lidocaine HCI 2% and epinephrine injection cartridges (50-count boxes) may have cracks or breaks in the containers. This defect could affect the sterility and safety of the medication. The affected lot D05362A expires July 31, 2027.

Novocol Pharmaceutical issued a recall of 2% Xylocaine Dental with Epinephrine 1:100,000 injection cartridges due to defective containers—some cartridges are cracked or broken. This affects lot D05337B (expires 06-30-2027). The problem was discovered during quality control; no injuries have been reported.

Olympia Provisions is recalling about 1,930 pounds of ready-to-eat holiday kielbasa sausage because metal fragments may be in the product. The sausages were produced on October 14, 2025, and sold in 16-ounce packages with a "best if used by" date of 02/19/26. No injuries have been reported so far.

Meaicezli Play Purse Sets contain toy cell phones and writing tablets with button or coin cell batteries that children can easily remove and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

Blue Wave above-ground pools 48 inches and taller have a compression strap around the outside of the pool legs that can act as a foothold, allowing children to climb into the pool unsupervised. This creates a serious drowning risk. The strap can provide access to the pool even if you remove the ladder.

ANNQUAN power strips (models EX-D112-05 and EX-D106-25) lack proper safety protection and can overheat and catch fire if overloaded. Seven units have blown fuses. The fire risk can cause serious injury or death from burns and smoke.

JOKOSIS bed rails (model HC0262) can trap users between the rail and mattress, creating a serious risk of entrapment and asphyxiation. The rails also lack required warning labels. About 12,000 units were sold on Amazon between August and November 2025.

KKL Fabric 9-Drawer Dressers can tip over and trap children if not anchored securely to the wall. The dressers do not meet federal safety standards for clothing storage units. About 4,740 units were sold on Amazon between September 2023 and November 2025.

Feel The Beard Beard Growth Oil contains minoxidil, a medication that must be in child-resistant packaging by law. The bottles do not have child-resistant caps, which means young children could open them and swallow the contents, causing serious injury or death. The product was sold online from April through September 2025.