Recalls in Utah (page 15)
3917 recalls.
- High Valley Orchard Chocolate Covered Raisins recall (Lehi Valley Trading Company, Inc)
FoodClass IReported July 15, 2026 · Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging. - Azacitidine for Injection 100mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Bortezomib for Injection 3.5mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Pemetrexed for Injection 500mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Pemetrexed for Injection 100mg/Vial recall (Reliance Life Sciences Private Limited)
DrugClass IIReported July 15, 2026 · Lack of Sterility Assurance - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Gasco Isopropyl Alcohol 70% recall (Gasco Industrial Corp.)
DrugClass IIReported July 15, 2026 · Subpotent drug - Methohexital Sodium recall (QuVa Pharma, Inc.)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications - Medline Remedy Specialized Silicone Cream recall (BioMed Laboratories, LLC.)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification. - Methohexital Sodium for Injection recall (ONESOURCE SPECIALTY PHARMA LIMITED)
DrugClass IIReported July 15, 2026 · Failed Impurities/Degradation Specifications - Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US ... recall (CMR SURGICAL LIMITED)
Medical deviceClass IIReported July 15, 2026 · Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. - OmniTract Surgical Retractor System recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported July 15, 2026 · The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be... - GSP Neonatal GALT Kit. Product Codes: 3303-001U recall (WALLAC OY)
Medical deviceClass IIReported July 15, 2026 · Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient... - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported July 15, 2026 · The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely... - 5008X Blood Tubing Set recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported July 15, 2026 · Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X... - KL Owen Custom Orthodontic Solution recall (Klowen Braces)
Medical deviceClass IIReported July 15, 2026 · A product error defect may cause incorrect bracket placement. - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in. recall (ConvaTec, Inc)
Medical deviceClass IIReported July 15, 2026 · Surgical dressing manufactured out of specification (greater thickness). - Olympus Single Use Distal Cover recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported July 15, 2026 · Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers. - Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Consumer productReported July 10, 2026 · Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit... - Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported July 10, 2026 · The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards. - WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Walmart.com by Wonder Stone Toys
Consumer productReported July 10, 2026 · The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a... - Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Yuezhang
Consumer productReported July 10, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
Consumer productReported July 10, 2026 · The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death. - Best Buy Recalls Insignia® Gas Ranges Due to Risk of Serious Injury from a Fire Hazard
Consumer productReported July 10, 2026 · The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard. - Conair Recalls Cuisinart Propel+ Four Burner 3-In-1 Gas Grills Due to Risk of Serious Injury from Laceration Hazard
Consumer productReported July 10, 2026 · The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard. - MorningStar Farms Hot & Spicy Sausage Patties recall (MARS SNACKING)
FoodClass IIReported July 8, 2026 · Potential contamination with plastic material - MorningStar Farms Buffalo Chik'n Nuggets recall (MARS SNACKING)
FoodClass IIReported July 8, 2026 · Potential contamination with plastic material - GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to catheter separation - Radius VSM Disposable NIBP Cuff recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Radius VSM ECG pre-connected Set recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code:... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - OTP5000 THORA/PARA TRAY recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 ... recall (Covidien LLC)
Medical deviceClass IIReported July 8, 2026 · Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP. - Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges recall (TELEFLEX LLC)
Medical deviceClass IIReported July 8, 2026 · Due to out-of-specification, or potential out-of-specification, levels of endotoxins - Short Monobloc Stem Broaches recall (Medacta Usa Inc)
Medical deviceClass IIReported July 8, 2026 · Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the... - Breathing circuit set recall (Hamilton Medical AG)
Medical deviceClass IReported July 8, 2026 · Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which... - a.) nara organics brand recall (NARA ORGANICS INC)
FoodClass IReported July 8, 2026 · Product may be contaminated with Clostridium botulinum. - MOGO PURE MORINGA OLEIFERA CAPSULES recall (MOGO Moringa LLC)
FoodClass IReported July 8, 2026 · Product may be contaminated with Salmonella Typhimurium - Glucagon Emergency Kit for Low Blood Sugar recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing. - Gemcitabine Injection recall (McKesson)
DrugClass IIReported July 8, 2026 · Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment. - Revitaderm Wound Care recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated - Fungal Fusion ERADICATION Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TERPENICOL Antifungal Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - vite20 Antifungal Cream recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TERPENICOL Antifungal Cream recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TRIPENICOL S Antifungal Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TRIFLUENT PHARMA TRIDERGEL Wound Care Gel recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated - Revitaderm Wound Care Gel recall (Blaine Labs Inc)
DrugClass IReported July 8, 2026 · Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Dextroamphetamine Saccharate recall (Lannett Company Inc.)
DrugClass IIReported July 8, 2026 · Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. - Lidocaine HCl Injection USP recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Accucaine recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported July 8, 2026 · Subpotent Drug - prednisoLONE Acetate Ophthalmic Suspension recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · Presence of Foreign Substance - Fexofenadine Hydrochloride Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported July 8, 2026 · Failed Impurities/Degradation Specifications - IMULDOSA recall (ACCORD BIOPHARMA INC)
DrugClass IIReported July 8, 2026 · Lack of assurance of Sterility: - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - ChloraPrep FREPP recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - Solar GI System recall (Laborie Medical Technologies Corp)
Medical deviceClass IIReported July 8, 2026 · Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's... - Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 recall (Carl Zeiss Meditec AG)
Medical deviceClass IIReported July 8, 2026 · Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the... - RayCare 2024A SP4. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - RayCare 2024A SP1. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - ARTIS icono floor. Model Number: 11327700. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono biplane. Model Number: 11327600. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - Adapter for Head Positioning recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported July 8, 2026 · The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of...