The Recall Desk

Archive

January 2024 recalls

524 recalls were announced in January 2024.

What the numbers show

Critical
12
Severe
125
High
295
Moderate
88
Low
4

Of the 524 recalls this month scored against our rubric, 2% are Critical, 24% are Severe.

Which agencies issued them

201–300 of 524

  • HighFDA (Devices)·Z-0728-2024·2024-01-24

    Ultrasound Examination Table Recall Due to Backrest Platform Stress Fracture

    Oakworks Inc is recalling Ultrasound EA examination tables because the backrest platform can develop stress fractures, making the table inoperable in inclined positions. Approximately 104 units distributed nationwide are affected.

    Product
    Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0754-2024·2024-01-24

    Suction Canister Liner Recalled for Loss of Suction on Low Settings

    Cardinal Health Suction Canister Liners may lose suction on low or intermittent settings due to liner misalignment. Approximately 3.5 million units are affected across the US, Canada, Australia, and New Zealand.

    Product
    CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0726-2024·2024-01-24

    PRIMA TT Shoulder Implant Baseplates Recalled for Manufacturing Defect Risk

    PRIMA TT shoulder implant baseplates are being recalled by Limacorporate due to manufacturing defects in the baseplate peripheral holes that could cause the implant to loosen or the screw to move.

    Product
    PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/1975.14.800, BASEPLATE D.25MM FULL WEDGED 10-degrees/1975.14.510, BASEPLATE D.28MM FULL WEDGED 10-degrees/1975.14.810, BASEPLATE
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0742-2024·2024-01-24

    Medex 700PSI Stopcock with Rotator Recalled Due to Seal Defect

    Smiths Medical is recalling Medex 700PSI stopcocks with rotators due to a manufacturing defect affecting the O-ring seal. The defect may cause medication leakage and under-infusion during patient treatment.

    Product
    Medex 700PSI STOPCOCK W/ROTATOR, List Number MX4331R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0761-2024·2024-01-24

    Maquet Operating Room Light Systems Recalled Due to Fall Risk

    Getinge USA Sales Inc is recalling Maquet Equipment OR Light Systems due to a potential risk that the light systems could fall in the operating room. Approximately 236,793 units have been distributed.

    Product
    Maquet Equipment OR Light Systems, Model Numbers and Catalog Numbers BRAINLAB CAMERA - ARDEQT269000A, BRAINLAB CAMERA - ARDEQT269000C, BRAINLAB CAMERA - ARDEQT269001A, BRAINLAB CAMERA - ARDEQT269001C, BRAINLAB CAMERA - ARDEQT269004A, BRAINLAB CAMERA - ARDEQT269004C, BRAINLAB CAME
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2024·2024-01-24

    Maquet Hanaulux HLX2000 Operating Room Lights Recalled Due to Fall Hazard

    Getinge Usa Sales Inc is recalling Maquet Hanaulux HLX2000 OR Light Systems because the light fixture may fall from its mounting in the operating room. Nearly 237,000 units are affected.

    Product
    Maquet Hanaulux HLX2000 OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3001 HXS12 - ARD567703001C, 4001 S/DF - ARD567211211C, 4001 SAD/DF - ARD567221211C, 4001 SAD/DF - ARD567221241C, 4001 SAD/SF - ARD567221141C, 4001 SAI/DF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0769-2024·2024-01-24

    Maquet G8 Operating Room Light Systems Recalled for Fall Risk

    Getinge USA is recalling Maquet G8 and G8E operating room light systems that may fall during use. Approximately 236,793 units have been distributed nationwide and globally.

    Product
    Maquet G8 / G8E OR Light Systems, Model Numbers and Catalog Numbers G8 LC E - ARD568131211C, G8G8 DF E - ARD568121111C, G8G8FS DF - ARD568121131C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0713-2024·2024-01-24

    Deli Carolina Style Mustard BBQ Sauce recalled for undeclared fish allergen

    Ventura Foods is recalling Deli Carolina Style Mustard BBQ Sauce for undeclared fish (anchovy) allergen. If you have a fish allergy, do not consume this product.

    Product
    DELI CAROLINA STYLE MUSTARD BBQ SAUCE, 2 oz (57g), plastic cup, 96 cups/case, store in ambient temperatures
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0757-2024·2024-01-24

    Maquet PowerLEDII Operating Room Light System Recalled for Fall Risk

    Getinge Usa Sales Inc is recalling Maquet PowerLEDII OR light systems due to a potential for the light to fall in the operating room. No injuries have been reported.

    Product
    Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWDII555DF - ARDPWT629101A, PWDII555SF - ARDPWT629102A, PWDII755DF - ARDPWT629103A, PWDII755SF - ARDPWT629104A, PWDII775DF - ARDPWT629105A, PWDII775SF - ARDPWT629106A, PWDII50DF - ARDPWT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2024·2024-01-24

    Intraocular Lens Cylinder Axis Marks Out of Specification

    Johnson & Johnson is recalling TECNIS Toric II intraocular lenses distributed in Japan. The cylinder axis marks do not meet product specifications and could affect vision correction.

    Product
    TECNIS Toric II OptiBlue IOL Models ZCW
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0750-2024·2024-01-24

    GammaPod Radiation Treatment Planning System Software Error Allows Wrong Imaging Structures

    Xcision Medical Systems recalled 4 GammaPod Treatment Planning Systems due to a software error that allows incorrect radiation structures from previous CT scans to be imported and selected, potentially affecting treatment planning accuracy.

    Product
    GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0740-2024·2024-01-24

    Medical Device Stopcock Recalled Due to O-Ring Seal Defect

    Smiths Medical Asd Inc is recalling approximately 31,685 Stopcock Left Rotator devices due to oversized O-rings that may compromise seal integrity. The defect may cause medication leaks, potentially resulting in under-infusion during treatment.

    Product
    1050 STOPCOCK LEFT ROTATOR OFF HANDLE, List Number MX1431MRL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0642-2024·2024-01-24

    ExcelsiusGPS surgical navigation system calibration error may cause device misplacement

    Globus Medical is recalling the ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit due to a calibration error that may cause inaccurate navigation and device misplacement during surgery. Nine units are distributed across select US states and internationally.

    Product
    ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit, Part number 6203.2100
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0718-2024·2024-01-24

    SOLTIVE SuperPulsed Laser Fibers May Have Breached Sterile Pouch Seals

    Olympus Corporation recalls 179 SOLTIVE SuperPulsed Laser Fibers due to potentially breached sterile pouch seals that could cause procedure delays or patient infections if not detected before use.

    Product
    SOLTIVE SuperPulsed Laser Fibers, Model No. TFL-FBX200BS
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0752-2024·2024-01-24

    Medical Diagnostic Calibration Serum Recalled for Positive Measurement Bias

    Randox Laboratories is recalling Calibration Serum Level 3 (CAL2351) distributed in the US and Puerto Rico because it exhibits a positive bias in CK Total measurements on RX Series instruments, potentially affecting test accuracy by up to 13%.

    Product
    Calibration Serum Level 3 CAL2351
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2024·2024-01-24

    Maquet PowerLED and PowerLED300 Surgical Light Systems Fall Hazard Recall

    Getinge recalls 236,793 units of Maquet PowerLED and PowerLED300 operating room light systems due to a potential for the light to fall in the operating room.

    Product
    Maquet PowerLED/HLED and PowerLED300 OR Light Systems, Model Numbers and Catalog Numbers EPS MB1 - ARDINT059002A, EPS MB1 - ARDINT059002C, EPS MB1 TR - ARDINT059000A, EPS MB1 TR - ARDINT059000C, EPS MB3 - ARDINT059003A, EPS MB3 - ARDINT059003C, EPS MB3 TR - ARDINT059001A, EPS MB3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0231-2024·2024-01-24

    Magnesium Citrate Oral Solution Recalled for Bacterial Contamination

    Pharma Nobis LLC is recalling 7,404 bottles of Freskaro Magnesium Citrate Oral Solution nationwide due to the presence of Acetobacter nitrogenifigens bacteria.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - CHERRY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0755-2024·2024-01-24

    Suction Canister Liners Recalled for Potential Loss of Suction Function

    Cardinal Health suction canister liners may lose suction on low settings due to liner misalignment. Approximately 203,244 units distributed to the US, Canada, Australia, and New Zealand.

    Product
    Cardinal Health MEDI-VAC CRD Suction Canister Liner, 1000 mL Suction Canister Liner Kit with 5 mm 1.8 m Tube, REF 65651-516
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0720-2024·2024-01-24

    Member's Mark Mild Cheddar Shredded Cheese Recalled for Glove Remnants

    Member's Mark Mild Cheddar shredded cheese is being recalled due to possible glove remnants. The recall affects specific lots distributed to Illinois, Indiana, Missouri, and Ohio.

    Product
    Member's Mark - Mild Cheddar Fancy (Fine) Shredded Cheese packaged in 5lbs, 8 packages per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0725-2024·2024-01-24

    Central Market Organic Chicken Broth Concentrate Recalled for Microbial Contamination

    TreeHouse Foods, Inc. is recalling Central Market 16oz Organic Low Sodium Chicken Broth Concentrate due to potential microbial contamination. The affected product has been distributed to 41 states.

    Product
    Central Market 16oz Organic Low Sodium Chicken Broth Concentrate
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0736-2024·2024-01-24

    Reduced Sodium Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling reduced sodium chicken broth sold under WinCo, HEB Select Ingredients, and Signature Select brands due to potential microbial contamination. Approximately 439,240 cases distributed to 37 states are affected.

    Product
    Reduced Sodium Chicken Broth labeled under: WinCo, 32oz Reduced Sodium Chicken Broth HEB Select Ingredients, 32oz Reduced Sodium Chicken Broth Signature Select, 48oz Reduced Sodium Chicken Broth Signature Select, 32oz Reduced Sodium Chicken Broth HEB Select Ingredients, 48oz Re
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0744-2024·2024-01-24

    Herold's Salads Cheddar Mac & Sour Cream recalled for Listeria contamination

    Herold Salads, Inc. is recalling Cheddar Mac & Sour Cream salads due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Cheddar Mac & Sour Cream packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0724-2024·2024-01-24

    Full Circle Organic Chai Tea Latte Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling Full Circle 32oz Organic Chai Tea Latte (Lot 98E03223) due to potential microbial contamination. The product was distributed across the U.S., and consumers should not consume it.

    Product
    Full Circle, 32oz Organic Chai Tea Latte
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0733-2024·2024-01-24

    Organic Chicken Bone Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling multiple brands of 32oz Organic Chicken Bone Broth due to potential microbial contamination. The affected products were distributed across 42 US states.

    Product
    Organic Chicken Bone Broth sold under: Culinary Treasures 32oz Organic Chicken Bone Broth Natures Promise 32oz Organic Chicken Bone Broth Sam's Choice 32oz Organic Chicken Bone Broth Simply Nature 32oz Organic Chicken Bone Broth Wild Harvest 32oz Organic Bone Broth Chicken
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0729-2024·2024-01-24

    Vegetable Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling vegetable broth sold under Essential Everyday, HEB Select Ingredients, and Chef's Cupboard brands due to potential microbial contamination. Products distributed to 37 states.

    Product
    Vegetable Broth sold under: Essential Every day, 32oz Vegetable Broth, HEB Select Ingredients, 32oz Vegetable Broth Chef's Cupboard, 32oz Vegetable Stock
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0727-2024·2024-01-24

    Organic Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling Organic Low/Reduced Sodium Chicken Broth sold under multiple brands due to potential microbial contamination. The recall affects 439,240 cases distributed across 37 states.

    Product
    Organic Low/Reduced Sodium Chicken Broth sold under: O Organics 32oz Organic Low Sodium Chicken Broth Central Market, 32oz Organic Low Sodium Chicken Broth Lidl, 32oz Organic Low Sodium Chicken Broth
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0773-2024·2024-01-24

    Cheddar Kettle Corn recalled due to undeclared milk allergen

    Sweet and Simple Kettle Corn is recalling Cheddar Kettle Corn because its label fails to declare milk as an ingredient. Consumers with milk allergies may be at risk from consuming this product.

    Product
    Cheddar Kettle Corn, Net Wt 10 Oz (283 g), Ingredients: Locally-Farmed Corn, Corn Oil, Sugar, Salt, 100% Cheddar Powder
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0712-2024·2024-01-24

    Wellsley Farms Assorted Mini Quiches Recalled for Possible Aluminum Foreign Material

    The Fillo Factory Inc. is recalling Wellsley Farms Assorted Mini Quiches due to possible aluminum foreign material contamination. Approximately 3,412 retail units distributed to stores across multiple states are affected.

    Product
    Wellsley Farms Assorted Mini Quiches NET WT 36 OZ (2LB 4 OZ) 1.02kb Keep Frozen UPC: 8867002630. Packaged in plastic trays in a cardboard box. 2 sealed trays in a box, 10 boxes per case
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0252-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled Due to Potential Benzene Contamination

    Procter & Gamble is recalling Old Spice SWEAT DEFENSE ULTIMATE CAPTAIN anti-perspirant spray due to potential benzene contamination at the manufacturing facility. Affected products have expiration dates through September 2023.

    Product
    Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum Chlorohydrate 23.5%, Anti-Perspirant, Topical spray can 3.8 OZ (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-385-10, UPC 0 37000 74947 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0229-2024·2024-01-24

    CVS Magnesium Citrate Oral Solution Recalled for Bacterial Contamination

    CVS Health Magnesium Citrate Saline Laxative Oral Solution in Grape flavor is being recalled due to microbial contamination with Acetobacter nitrogenifigens bacteria. Affected lot A80763 (expiration 11/2025) was distributed nationwide.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (CVS MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0255-2024·2024-01-24

    Secret Dry Spray Antiperspirant Recalled Due to Manufacturing Facility Contamination Risk

    The FDA is recalling certain lots of Secret Dry Spray Antiperspirant due to a manufacturing facility deviation and potential benzene contamination. All affected lots expire through September 2023.

    Product
    Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0723-2024·2024-01-24

    Endoscopic Vessel Harvesting System Recalled Due to Polyimide Particulate Matter Risk

    Maquet Cardiovascular is recalling the Vasoview Hemopro Endoscopic Vessel Harvesting System (model VH-3000-W) because polyimide particulate matter may be present on the device and could be introduced into arterial conduits during bypass graft surgery.

    Product
    Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0748-2024·2024-01-24

    SOLTIVE SuperPulsed Laser Fibers Recalled for Potential Fiber Breakage During Surgery

    Olympus is recalling 82,200 units of SOLTIVE SuperPulsed Laser Fibers due to instruction inconsistencies that could cause fiber breakage during use, potentially resulting in burns or foreign material in the patient.

    Product
    SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S, TFL-FBX200S, TFL-FBX365S, TFL-FBX550S, TFL-FBX940S, TFL-FBX150BS, TFL-FBX200BS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0716-2024·2024-01-24

    Olympus Laser Fiber Stripper Recall Due to Sterilization Validation Gap

    Olympus recalls fiber stripper models sold before 2023 lacking validated sterilization instructions, creating a contamination risk when used on sterile medical fibers.

    Product
    Soltive SuperPulsed Laser System TFL Fiber Stripper, Model Numbers TFL-AFS150, TFL-AFS200, TFL-AFS365, TFL-AFS550, TFL-AFS940
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0770-2024·2024-01-24

    Maquet Blueline Series OR Light Systems Recalled Due to Fall Risk

    Getinge Usa Sales Inc is recalling Maquet Blueline Series 30/80 operating room light systems that may fall in the operating room. No injuries have been reported.

    Product
    Maquet Blueline Series 30/80 OR Light Systems, Model Numbers and Catalog Numbers BLUE 30 - ARD569015111A, BLUE 30 - ARD569015111C, BLUE 30 - ARD569015131C, BLUE 30 - ARD569025111C, BLUE 30 - ARD569025131C, BLUE 30 - ARD569035111C, BLUE 30 - ARD569035131C, BLUE 30 - ARD569045111C,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0760-2024·2024-01-24

    Maquet Rolite OR Light Systems Recall Due to Fall Risk

    Getinge USA is recalling 236,793 Maquet Rolite operating room light systems due to a potential for the light fixture to fall. No injuries have been reported.

    Product
    Maquet Rolite OR Light Systems, Model Numbers and Catalog Numbers ROL PWDII50SF - ARDPWT309001A, ROL PWDII50SF - ARDPWT309002A, ROL PWDII50SF - ARDPWT309009A, ROL PWDII50SF - ARDPWT309010A, ROL PWDII70SF - ARDPWT309007A, ROL PWDII70SF - ARDPWT309008A, ROL PWDII70SF - ARDPWT309015
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0747-2024·2024-01-24

    Smiths Medical Injection Line Rotating Adapters Recalled for Seal Defect

    Smiths Medical is recalling specific injection line rotating adapters due to a manufacturing defect causing oversized O-rings that may lead to inadequate seal integrity and medication under-infusion.

    Product
    48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi), List Number MX694R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0756-2024·2024-01-24

    Cardinal Health Suction Canister Liners may lose suction due to misalignment

    Cardinal Health Medi-Vac suction canister liners in specific lots may lose suction on low settings due to misalignment of the liner with the outer canister. Stop using affected units and contact the manufacturer for replacements.

    Product
    Cardinal Health Suction Canister Liner, MEDI-VAC CRD 1000 mL Suction Canister Liner Kit with 6 mm 1.8 m Tube, REF 65651-517
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0719-2024·2024-01-24

    Incisive CT systems with ECG cable risk of signal loss

    Philips Incisive CT systems with specific ECG cable may experience signal loss due to connector weakness, potentially delaying diagnosis.

    Product
    Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-0731-2024·2024-01-24

    Philips Patient Information Center iX: Push Notifications May Fail to Send

    Philips Patient Information Center iX devices may fail to send push notifications under certain conditions, potentially delaying detection of patient condition changes. A total of 814 units have been recalled worldwide.

    Product
    (1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0743-2024·2024-01-24

    High Pressure Rotator Infusion Device Recalled Due to Seal Defect

    Smiths Medical is recalling 31,685 HIGH PRESSURE ROTATOR infusion devices with a manufacturing defect that may cause an inadequate seal. The defect could lead to medication leaks and under-infusion.

    Product
    HIGH PRESSURE ROTATOR WITH MALE LUER LOCK, List Number MX496HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2024·2024-01-24

    Maquet Hanaulux HLX3000 Operating Room Light Systems Recall for Fall Hazard

    Getinge Usa Sales Inc is recalling approximately 236,793 Maquet Hanaulux HLX3000 operating room light systems nationwide and globally due to a potential for the light system to fall in the operating room.

    Product
    Maquet Hanaulux HLX3000 OR Light Systems, Model Numbers and Catalog Numbers H3 BC - HM567811111C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0764-2024·2024-01-24

    Maquet Axcel Operating Room Light Systems Recalled for Fall Hazard

    The FDA is recalling Maquet Axcel and Axcel+ operating room light systems due to a potential for the light system to fall. The recall affects 236,793 units distributed nationwide and globally.

    Product
    Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD567505961C, AXL 5002 - ARD567501962C, AXL 5002S - ARD567505962C, AXL 5501 - ARD567501960A, AXL 5501 - ARD567501960C, AXL 5501S - ARD567505960C, AXL+5001 DF - ARD567
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0771-2024·2024-01-24

    Maquet Operating Room Light Systems Recalled Due to Fall Hazard

    Getinge Usa Sales Inc is recalling 236,793 Maquet operating room light systems nationwide due to a potential for the light system to fall, posing a safety risk to surgical patients and staff.

    Product
    Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Numbers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0744-2024·2024-01-24

    High Pressure Rotator with O-Ring Seal Defect Recalled Worldwide

    Smiths Medical is recalling High Pressure Rotators due to a manufacturing defect affecting O-ring seals. An oversized inner diameter may cause inadequate seal integrity, risking medication under-infusion.

    Product
    HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0767-2024·2024-01-24

    Maquet Prismalix OR Light Systems recalled due to fall hazard

    Getinge has recalled 236,793 Maquet Prismalix operating room light systems because the systems could potentially fall. The recall affects units distributed nationwide in the U.S. and globally.

    Product
    Maquet Prismalix OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3001 HXS12 - ARD567703001C, 4001 S/DF - ARD567211211C, 4001 SAD/DF - ARD567221211C, 4001 SAD/DF - ARD567221241C, 4001 SAD/SF - ARD567221141C, 4001 SAI/DF - ARD56
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0730-2024·2024-01-24

    Ultrasound Examination Table Recalled for Backrest Stress Fracture

    Oakworks Inc is recalling 28 Ultrasound EA examination tables due to backrest platform stress fractures that prevent operation in an inclined position.

    Product
    Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2024·2024-01-24

    Field Cricothyrotomy Kit Recalled for Incompatible Endotracheal Tube Holder

    Sarnova HC is recalling the Curaplex Field Cric Kit due to an incompatible endotracheal tube holder that prevents practitioners from securing the tube during cricothyrotomy procedures. The recall affects 1,063 kits distributed nationwide.

    Product
    Curaplex Field Cric Kit with ET Tube, Item Number 36611. The kit provides healthcare professionals with an assortment of supplies to perform a cricothyrotomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0745-2024·2024-01-24

    Braided Injection Line Recalled for Potential Medication Leaks

    Smiths Medical is recalling approximately 31,685 units of a braided injection line due to manufacturing defects in the O-ring seal. The defect may cause medication leaks that reduce drug delivery.

    Product
    20IN (50.8CM) BRAIDED INJ LINE, ROTATING ADAPT, List Number MX682BR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0717-2024·2024-01-24

    Medical Fiber Cleaver System Recalled for Contamination Risk

    Olympus Corporation recalled 236 fiber cleaver units distributed non-sterile but labeled as reusable and autoclavable. Without validated sterilization instructions, use on sterile fiber poses contamination risk.

    Product
    Soltive SuperPulsed Laser System TFL FIBER CLEAVER, Model Number TFL-AFC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0725-2024·2024-01-24

    Philips Spectral CT 7500 Recalled for Multiple Software Issues Affecting Functionality

    Philips is recalling 197 Spectral CT 7500 computed tomography systems due to multiple software issues affecting device functionality. The devices were distributed nationwide and internationally.

    Product
    Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2024·2024-01-24

    Maquet Orchide OR Light Systems recalled due to fall risk

    Getinge USA is recalling Maquet Orchide OR Light Systems due to a potential for light fixtures to fall in the operating room. No injuries have been reported.

    Product
    Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD56880
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0726-2024·2024-01-24

    Organic Chicken Broth Recalled Nationwide for Potential Microbial Contamination

    TreeHouse Foods is recalling multiple brands of organic chicken broth due to potential microbial contamination. Approximately 439,240 cases were distributed across 37 states.

    Product
    Organic Chicken Broth sold under: 365 Organic, 32oz Chicken Broth, Good & Gather, 32oz Organic Chicken Broth Sprouts, 32oz Organic Chicken Broth Natures Promise, 32oz Organic Chicken Stock Market Basket, 32oz Organic Chicken Stock O Organics, 32oz Organic Chicken Broth
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Food)·F-0732-2024·2024-01-24

    Central Market Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods recalls Central Market 32oz Organic No Salt Added Chicken Broth (lot code 98C06193) for potential microbial contamination affecting 439,240 cases distributed across 41 states.

    Product
    Central Market 32oz Organic No Salt Added Chicken Broth
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-0736-2024·2024-01-24

    BD PosiFlush Prefilled Saline Syringes Recalled for Incorrect Stopper

    Becton Dickinson is recalling 5,085,120 BD PosiFlush Prefilled Saline Syringes due to an incorrect stopper that increases injection force and may trigger pump alarms.

    Product
    PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0722-2024·2024-01-24

    Chicken Broth Recalled for Potential Microbial Contamination

    TreeHouse Foods is recalling 439,240 cases of chicken broth products sold under multiple brands for potential microbial contamination. Products were distributed across 37 states.

    Product
    Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken Broth, UPC: 50428430095, carton H-E-B, 48oz Chicken Broth, UPC: 41220610013, carton HEB Select Ingredients, 32oz Chicken Broth, UPC: 41220610006, 41220610075 (cl
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Drugs)·D-0230-2024·2024-01-24

    Freskaro Magnesium Citrate oral solution recalled for bacterial contamination

    Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor) nationwide due to the presence of Acetobacter nitrogenifigens bacteria.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0737-2024·2024-01-24

    V. Mueller Bandage Scissors recalled for pink dye staining on handles

    Steris Corporation is recalling V. Mueller Universal Bandage Scissors (Model SU2014-001) due to an incorrect resin carrier in the handle cover. Pink dye residue may appear on scissors and sterilization pouches after processing.

    Product
    V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through tape and bandages Model: SU2014-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V036000·2024-01-23

    Tiffin motorhome driver seat pedestal plates may be improperly welded

    Tiffin is recalling certain 2022 motorhomes because the pedestal mounting plate on the driver's seat may be improperly welded, allowing the seat assembly to loosen or detach. 507 units affected.

    Product
    TIFFIN — TIFFIN ALLEGRO RED 360, ALLEGRO BUS, ZEPHYR, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V038000·2024-01-23

    Suzuki Recalls 2024 GSX1300R Motorcycles Due to Brake Fluid Leak Risk

    Suzuki is recalling 2024 GSX1300R motorcycles because an incorrectly tightened brake fluid pipe flare nut may cause a leak, reducing braking performance and increasing crash risk.

    Product
    SUZUKI — SUZUKI GSX1300R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V037000·2024-01-23

    Brinkley Model Z axle spindle welds may fail and detach wheels

    Brinkley RV is recalling certain 2024 Model Z recreational vehicles because the axle spindle weld may fail, resulting in the wheel assembly detaching from the axle. 17 units affected.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V028000·2024-01-19

    Marion Fire Apparatus Recalled for Electrical Wiring Fire Risk

    Marion Body Works is recalling 2020-2022 fire apparatus vehicles due to a firmware defect that can cause electrical circuits to overheat and increase fire risk.

    Product
    MARION — MARION PUMPER, RPM, AERIAL, RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V030000·2024-01-19

    Forest River Recalls 2024 Shasta Oasis Trailers for Lighting Defect

    Forest River is recalling 2024 Shasta Oasis travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers.

    Product
    SHASTA — SHASTA OASIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V032000·2024-01-19

    Maxi-Metal Recalls 2020-2023 Kenworth and Freightliner Trucks for Fire Risk

    Maxi-Metal is recalling 2020-2023 Kenworth and Freightliner trucks because a firmware defect in certain electrical nodes may prevent circuits from shutting off, increasing the risk of fire.

    Product
    MAXI-METAL — MAXI-METAL KENWORTH, FREIGHTLINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V033000·2024-01-19

    Nova Bus Recalls 2017-2019 LFS Models for Door Window Marking Defect

    Nova Bus is recalling 2017-2019 LFS and LFS Artic buses because driver's door windows may have incorrect DOT code marks, potentially leading to improper glass replacement and reduced visibility.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V029000·2024-01-19

    2024 Forest River IBEX trailers recalled for suspension fastener safety

    Forest River is recalling certain 2022–2024 IBEX, NO BOUNDARIES, and R-POD trailers because fasteners for the independent suspension may loosen and allow the suspension to detach, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER IBEX, R-POD, NO BOUNDARIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24084·2024-01-18

    Home Design Upholstered Low Profile Beds Recalled for Fall Injury Risk

    Home Design is recalling about 527,177 upholstered low-profile beds sold through Wayfair, Walmart.com, and Overstock.com from July 2018 through November 2023. The beds can break, sag, or collapse during use, creating a fall and injury hazard.

    Product
    Upholstered Low Profile Standard and Platform Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V026000·2024-01-18

    Navistar Recalls 2024 International HV and MV Trucks for Seat Belt Defect

    Navistar is recalling 2024 International HV and MV trucks because the driver's seat belt tether bolt may not be properly seated, increasing injury risk in a crash.

    Product
    INTERNATIONAL — INTERNATIONAL HV, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V021000·2024-01-18

    Lode King Trailers Recalled for Anti-Lock Brake System Defect

    Lode King is recalling specific AHV45-3 and Prestige trailers because reversed ABS sensor connections may reduce braking effectiveness during wheel lockup.

    Product
    LODE KING — LODE KING AHV45-3, PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V025000·2024-01-18

    2023 and 2024 Kia Carnival vehicles recalled for loose roof molding

    Kia is recalling certain 2023–2024 Carnival and 2023–2024 Sportage vehicles because the roof molding may loosen and detach, creating a road hazard for other vehicles.

    Product
    KIA — KIA CARNIVAL, SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24086·2024-01-18

    Steamist Wall-Mounted Tilt-Up Bath Shower Seats Recalled for Fall and Laceration Hazards

    Steamist is recalling about 3,900 wall-mounted, folding teak wood shower seats because the support rods and mounting brackets can corrode and break, creating fall and laceration hazards. The firm has received 62 reports of the seats breaking, including 4 injury reports.

    Product
    Tilt-Up Bath & Shower Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V023000·2024-01-18

    2018–2022 Land Rover Range Rover and Range Rover Sport rearview camera recall

    Jaguar Land Rover is recalling certain 2018–2022 Range Rover and Range Rover Sport vehicles because water may enter the rearview camera, causing it to fail to display or show a distorted image, reducing rear visibility while in reverse.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V027000·2024-01-18

    Navistar Recalls 2024 IC EV School Buses for Mislabeled Cables

    Navistar is recalling 2024 IC EV school buses because high-voltage cables may be mislabeled, posing an electrical shock risk to technicians.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24085·2024-01-18

    Bokser Home 100% Cotton Mattress Pads Recalled for Fire Hazard

    Bokser Home is recalling about 2,300 units of 100% cotton mattress pads because they violate federal flammability regulations and pose a fire hazard. No injuries have been reported.

    Product
    Bokser Home 100% Cotton Mattress Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01182024-02·2024-01-18

    USDA Issues Public Health Alert for Ready-to-Eat Charcuterie Products

    USDA FSIS issued a public health alert for Busseto and Fratelli Beretta charcuterie products due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    Fratelli Beretta USA, INC. — FSIS Issues Public Health Alert for Ready-To-Eat Charcuterie Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01182024-01·2024-01-18

    USDA Issues Public Health Alert for Uninspected Raw Frozen Pork Dumplings

    USDA FSIS issued a public health alert for raw frozen pork dumplings produced without federal inspection. No illnesses have been reported, but consumers are urged to discard the products.

    Product
    Dim Sum Factory, Inc. — FSIS Issues Public Health Alert for Raw Frozen Pork Dumpling Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0700-2024·2024-01-17

    Eban's Bakehouse Turtle Brownie Cookies Recalled for Undeclared Milk and Soy

    Eban's Bakehouse LLC is recalling Turtle Brownie cookies that contain undeclared milk and soy allergens. Consumers with allergies should not consume the product.

    Product
    Eban's Bakehouse Sweet Indulgences - Turtle Brownie (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereNHTSA·24V020000·2024-01-17

    Morgan Super 3 motorcycles recalled for brake master cylinder weld defect

    Morgan Motor Company is recalling 2023 Super 3 motorcycles because a defective weld may cause brake failure. Owners should contact the manufacturer for a free repair.

    Product
    MORGAN MOTOR COMPANY — MORGAN MOTOR COMPANY SUPER 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0696-2024·2024-01-17

    Eban's Bakehouse cookies recalled for undeclared milk and soy allergens

    Eban's Bakehouse Sweet Indulgences Brown Butter Snickerdoodles are recalled due to undeclared milk and soy allergens. The FDA Class I recall affects 876 units distributed to 33 states.

    Product
    Eban's Bakehouse Sweet Indulgences - Brown Butter Snickerdoodle (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0694-2024·2024-01-17

    Eban's Bakehouse Sweet Indulgences cookies recalled for undeclared milk and soy

    Eban's Bakehouse LLC is recalling Sweet Indulgences cookies for containing undeclared milk and soy allergens, which pose serious health risks to allergic consumers.

    Product
    Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Drugs)·D-0220-2024·2024-01-17

    Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk

    InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.

    Product
    VIGABATRIN — VIGABATRIN (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0703-2024·2024-01-17

    Maple Nut Fudge Recalled Due to Undeclared Egg Allergen

    Valley View Candies is recalling Maple Nut Fudge 8oz containers due to undeclared egg allergen. The product was distributed to retail stores in Iowa.

    Product
    Maple Nut Fudge, 8oz, packaged in clear, plastic clamshell.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0697-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse has recalled Sweet Indulgences Chocolate Chili Coconut cookies due to undeclared milk and soy allergens. The product was distributed nationwide and poses a risk to allergic consumers.

    Product
    Eban's Bakehouse Sweet Indulgences - Chocolate Chili Coconut (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0699-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse Sweet Indulgences cookies are recalled due to undeclared milk and soy allergens not listed on the label. Consumers with allergies to milk or soy should not consume this product.

    Product
    Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate Chunk (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0695-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse Sweet Indulgences cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies should not consume these products and should discard or return them.

    Product
    Eban's Bakehouse Sweet Indulgences - Brown Butter Honey Pistachio (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0698-2024·2024-01-17

    Eban's Bakehouse Lemon Sugar Cookies Recalled for Undeclared Milk and Soy

    Eban's Bakehouse Sweet Indulgences lemon cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Eban's Bakehouse Sweet Indulgences - Lemon Sugar Cookie/Lemon Shortbread (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0704-2024·2024-01-17

    Peanut Butter Fudge Recalled for Undeclared Egg Allergen

    All lots of Peanut Butter Fudge sold in Iowa are recalled due to undeclared egg allergen. The manufacturer initiated the voluntary recall.

    Product
    Peanut Butter Fudge, 8oz, packaged in clear, plastic clamshell.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0701-2024·2024-01-17

    FDA recalls Chocolate Fudge for undeclared egg allergen

    Valley View Candies recalled Chocolate Fudge due to undeclared egg allergen. The recall affects 348 containers distributed to retail stores in Iowa.

    Product
    Chocolate Fudge, 8oz, packaged in clear, plastic clamshell.
    Category
    Food
    Distribution
    1 state

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