Wyoming recalls

Zimmer has recalled a plastic reamer guide used in shoulder surgery because the plastic can catch and break during the reaming procedure. Five complaints have been received describing this issue. No injuries have been reported.

PFM Medical's Multi-Snare Set catheters (5 mm and 10 mm models) failed to meet biocompatibility safety standards. If used, the device material could cause localized inflammation and tissue irritation when in contact with blood vessels.

Ventec Life Systems' VOCSN+Pro respiratory ventilator may have a damaged backup battery that powers the alarm system. If primary power is lost and the backup battery is depleted or absent, the backup alarm may not sound to alert caregivers of the power loss.

TMJ Solutions Inc. has recalled one custom temporomandibular joint implant (model CHG020) that may contain incorrect patient-specific components. The mismatch caused a poor fit, resulting in a right-sided open bite for the affected patient.

Certain Philips Avalon FM 30 fetal monitors have an incorrect speaker connector assembly that can allow device cables to be pulled out of the housing. This defect may cause the speaker to stop working intermittently or permanently, which could affect audio output during monitoring.

Certain Philips Avalon FM20 Fetal Monitors have a speaker connector that was assembled incorrectly. This defect can cause cables to pull out of the device housing, which may result in loss of speaker output—either intermittently or permanently. This affects audio alerts that are critical to clinical monitoring.

Certain Da Vinci surgical systems were distributed with a defective E-brake retainer pin. If the structural column fails, this pin can prevent the E-brake from engaging, potentially causing uncontrolled motion of the robotic arm. The pin may also loosen or back out, restricting arm movement or causing uncontrolled motion that could injure patient tissue.

Medline Convenience Kits containing anesthetic medications (Lidocaine and Bupivacaine injections) were recalled due to quality issues found during an FDA inspection of the supplier. The affected kits are used in medical procedures including central line placement and open heart surgery.

Medline Convenience Kits containing Arrow Kits and Sets with Lidocaine and Bupivacaine anesthetic injections were recalled due to quality issues found during an FDA inspection of the supplier. The kits are used for central and arterial line procedures in medical settings. A total of 233 units were distributed nationwide.

Medline Convenience Kits used in cardiac surgery contain anesthetic medications (Lidocaine and Bupivacaine) that were recalled by their supplier due to quality concerns found during an FDA inspection. About 6,775 affected kits have been distributed to hospitals and surgical centers.

Medline Convenience Kits used in cardiovascular anesthesia room setups contain anesthesia injectables (Lidocaine and Bupivacaine) that were recalled due to quality problems found during an FDA inspection of the supplier. The affected kits are used in hospital operating rooms.

Undeclared allergens: Milk and Soy

Spring & Mulberry Blood Orange Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is sold individually and in multi-packs on Amazon, as well as in wholesale cases. Three specific lot codes and use-by dates are involved.

Spring & Mulberry Coffee Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is sold individually and in multi-packs on Amazon, as well as through wholesale distribution. The recall includes specific lot numbers with use-by dates ranging from February to June 2027.

Spring & Mulberry Sea Salt Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is a 2.1 oz bar sold individually or in multi-packs, with specific batch/lot numbers 026013 and 026014, use-by date 07/31/2027, and UPC 850055470071.

Spring & Mulberry Pure Dark and Pure Dark Minis chocolate bars may be contaminated with Salmonella. The affected products were distributed nationwide in individual bars and multi-packs. No illnesses have been reported.

Spring & Mulberry Pecan Date Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects specific batches with expiration dates ranging from August 2026 through December 2026. The bars are sold individually and in multi-packs on Amazon.

Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is sold individually and in multi-packs (3, 6, or 12-packs) on Amazon, as well as wholesale.

Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects approximately 17,848 individual bars sold nationwide, including bars sold on Amazon in single and multi-packs.

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars may be contaminated with Salmonella. The recall affects specific batch lots with use-by dates ranging from January through August 2027. No illnesses have been reported.

Spring & Mulberry Earl Grey Date-Sweetened Chocolate bars may be contaminated with Salmonella. The affected product is a 2.1 oz. chocolate bar in a purple box sold individually and in multi-packs on Amazon, with specific lot numbers and use-by dates identified.

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars (2.1 oz) may be contaminated with Salmonella. The affected product was distributed nationwide and sold individually and in multi-packs on Amazon. Salmonella can cause serious illness.

Potential Salmonella contamination

Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.

Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.

Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.

Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.

BD ChloraPrep FREPP Clear, a sterile skin antiseptic applicator, may contain fungal contamination (Aspergillus penicillioides) or may not be fully sterile due to wrinkles in the packaging seal. Approximately 178,000 applicators from lot 4073005 (expiring 03/31/2027) are affected nationwide and internationally.

BD ChloraPrep Clear, a sterile antiseptic skin-prep solution used before medical procedures, was found to contain Aspergillus penicillioides fungus in some applicators. This affects the sterility of the product, which is critical for medical use. The affected lot is Lot #4032183 with an expiration date of January 31, 2027.

BD ChloraPrep FREPP Clear applicators may have wrinkles in the paper lid that could compromise the sterile seal. This affects multiple lot numbers distributed nationwide through mid-2027. No injuries have been reported.