The Recall Desk

Archive

September 2022 recalls

527 recalls were announced in September 2022.

What the numbers show

Critical
21
Severe
145
High
306
Moderate
53
Low
2

Of the 527 recalls this month scored against our rubric, 4% are Critical, 28% are Severe.

Which agencies issued them

201–300 of 527

  • HighFDA (Devices)·Z-1723-2022·2022-09-21

    ICU Medical IV Connector Extension Set Recalled for Manufacturing Defect

    ICU Medical is recalling intravascular administration set connectors due to a manufacturing defect that creates a visible gap in the connector housing. The defect affects approximately 5.8 million units distributed nationwide and internationally.

    Product
    6.5 IN (17 cm) APPX 0.78 ml, EXT SET w/Clave CLEAR, Clave 4-WAY Stopcock, Spiros, RED CAP. Accessory for intravascular administration set.
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-1708-2022·2022-09-21

    Roadrunner PC Hydrophilic Wire Guide Recalled Due to Sterility Testing Failure

    Cook Incorporated is recalling 1,450 units of Roadrunner PC Hydrophilic Wire Guide devices due to failed sterility packaging testing. The devices may not meet sterility requirements for safe use in vascular procedures.

    Product
    Roadrunner PC Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN):RLPC-35-180 ORDER NUMBER (GPN) G07516. For vascular catheter positioning and exchange in diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1724-2022·2022-09-21

    ICU Medical Trifuse Extension Set Recalled for Connector Housing Gap

    ICU Medical is recalling 5.8 million Trifuse Extension Sets due to a manufacturing defect that creates a visible gap between the connector's housing parts. The gap could lead to disconnection or fluid leakage during infusion.

    Product
    6" (15 cm) Appx 0.85 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 2 Check Valve, 3 Clamps, Rotating Luer;
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-1727-2022·2022-09-21

    GXL Acetabular Liners Recalled Due to Non-Conforming Packaging

    Exactech recalled 132 GXL acetabular liners (hip implant components) due to non-conforming bags that may accelerate device wear. Units were distributed worldwide to the US and 13 countries.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH +5MM LAT LINER 15 DEG 36MM ID, SIZE H, REF 138-36-08 b. ACUMATCH +5MM LAT LINER 15 DEG 36MM ID, SIZE J, REF 138-36-09 c. ACUMATCH LINER 15 DEG 36MM ID, SIZE H, REF 132-36-08 d. ACUM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1719-2022·2022-09-21

    Medical connector recalled due to manufacturing housing gap defect

    ICU Medical is recalling MicroClave Clear Neutral Connectors used in intravascular catheters due to a manufacturing defect that creates a visible gap between housing parts.

    Product
    MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed in the vein or artery.
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-1739-2022·2022-09-21

    Isopure ACDS Hemodialysis Equipment Recalled for Electrical Shock Risk

    Isopure Corp recalls its ACDS (Acidified Concentrate Distribution and Storage) system used in hemodialysis facilities due to a potential electrical safety hazard that may result in electric shock or arcing.

    Product
    Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified Concentrate Distribution and Storage) with remote fill is intended to be used in Hemodialysis facilities for the storage and distribution of acid concentrate to be used in the treatment of Hemodialysis p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1731-2022·2022-09-21

    GXL Acetabular Liners Packaged Improperly May Experience Accelerated Wear

    Exactech is recalling certain GXL acetabular hip implant liners because non-conforming packaging may cause accelerated wear. No injuries have been reported.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. GXL NEUTRAL LINER, G0 28MM ID, 130-28-50; b. GXL NEUTRAL LINER, G00 22MM ID, 130-22-70; c. NOVATION GXL LIPPED LINER, G0 28MM ID, 132-28-50; d. NOVATION GXL LIPPED LINER, G00 22MM ID, 132
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1751-2022·2022-09-21

    iSED Tubing Spare Part Recalled for Potential Biohazard Leak Risk

    Alcor Scientific is recalling iSED Primary Pump Tubing Spare Part Kits due to potential biohazard leak from the Probe Tube when installed on the iSED ESR Analyzer. Affected lot (4/22) includes 38 units distributed nationwide and internationally.

    Product
    iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is used to move sample and wash solution from the aspiration needle, through the reading chamber, and to the waste on the iSED Automated ESR Analyzer PN: 112-13-002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1750-2022·2022-09-21

    Surpria 64 Software Error May Prevent Image Reconstruction During Scanning

    Surpria 64 CT scanner software versions V3.11 and V3.22 may encounter errors that prevent image reconstruction, requiring repeat scans that expose patients to additional radiation. 16 units nationwide are affected.

    Product
    Surpria 64: Software Version V3.11, V3.22
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1710-2022·2022-09-21

    Vascular Catheter Wire Guide Recalled for Possible Sterility Compromise

    Cook Incorporated is recalling 585 Roadrunner UniGlide Hydrophilic Wire Guides because they failed packaging sterility tests, potentially compromising device sterility.

    Product
    Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPW-35-150 ORDER NUMBER (GPN):G56149. For vascular catheter positioning and exchange in diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1734-2022·2022-09-21

    GXL Acetabular Liners Packaging Defect May Cause Accelerated Wear

    Exactech GXL acetabular hip implant liners in non-conforming bags may experience accelerated wear. Approximately 7,946 devices were distributed worldwide. No injuries have been reported.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH 0 DEGREE LINER 28MM 46MM, REF 130-28-05; b. ACUMATCH 0 DEGREE LINER 28MM 48MM, REF 130-28-06; c. ACUMATCH 0 DEGREE LINER 28MM 50/52MM, REF 130-28-07; d. ACUMATCH 0 DEGREE LINER 28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1726-2022·2022-09-21

    GXL Acetabular Liners Recalled Due to Improper Packaging and Accelerated Wear

    Exactech is recalling 136 GXL acetabular liners used in hip implants due to non-conforming packaging that may cause accelerated wear. The devices were distributed worldwide to multiple countries.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH 15 DEGREE LINER 22MM SZ C, REF 132-22-03 b. ACUMATCH 15 DEGREE LINER 28MM SZ D, REF 13-28-04
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1707-2022·2022-09-21

    Roadrunner PC Hydrophilic Wire Guide Recalled Due to Packaging Integrity Failure

    Cook Incorporated is recalling 2,407 units of Roadrunner PC Hydrophilic Wire Guide due to failed packaging integrity testing that may compromise device sterility. No illnesses or injuries have been reported.

    Product
    Roadrunner PC Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): RFSPC-35-180 ORDER NUMBER (GPN) G09608. For vascular catheter positioning and exchange in diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1749-2022·2022-09-21

    FUJIFILM Surpria Imaging Software May Fail During Scanning

    Surpria software versions V3.11 and V3.22 may encounter processing errors that prevent image reconstruction, potentially requiring additional scans and exposing patients to unnecessary radiation.

    Product
    Surpria: Software Version V3.11, V3.22
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1716-2022·2022-09-21

    Roadrunner UniGlide wire guide recalled for potential sterility compromise

    Cook Incorporated is recalling 189 Roadrunner UniGlide hydrophilic wire guides because they failed packaging testing requirements and their sterility may be compromised.

    Product
    Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWAS-35-80 ORDER NUMBER (GPN): G56175. For vascular catheter positioning and exchange in diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1745-2022·2022-09-21

    INOmax DSIR Delivery System incompatible with upgraded Leoni Plus ventilator

    The INOmax DSIR nitric oxide delivery system is incompatible with the 2021-upgraded Leoni Plus ventilator. Without proper connection including a required one-way valve, patients may receive excessive nitric oxide.

    Product
    INOmax DSIR -(delivery system) delivers INOMAX (nitric oxide for inhalation) therapy gas into the inspiratory limb of the patient breathing circuit in a way that provides a constant concentration of nitric oxide (NO), as set by the user, Model Number: 10007
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1730-2022·2022-09-21

    GXL Acetabular Liners Recalled Due to Non-Conforming Packaging and Accelerated Wear Risk

    Exactech's GXL acetabular hip implant liners are being recalled because they were packaged in non-conforming bags that may cause accelerated wear of the devices.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. NOVATION CONSTRAINED LINER 28MM ID GROUP 1, REF 134-28-41 b. NOVATION CONSTRAINED LINER 32MM ID GROUP 2, REF 134-32-42 c. NOVATION CONSTRAINED LINER 36MM ID GROUP 3, REF 134-36-43 d.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22E079000·2022-09-21

    Skinny Guy Campers Recalls Model 6.5 Campers Due to LP Gas Leak Risk

    Skinny Guy Campers is recalling Model 6.5 Campers because cracked quick disconnect fittings in the LP gas system may cause a gas leak, increasing fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1515-2022·2022-09-21

    L-Carnitine Injectable Recalled Due to Sterility Assurance Failure

    Carolina Infusion is recalling L-Carnitine 500 mg/mL injectable vials nationwide due to lack of assurance of sterility. The affected lot 06132022@17 should not be administered.

    Product
    L-Carnitine 500 mg/mL Injectable, 10 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V707000·2022-09-21

    2022-2023 Volkswagen Golf R and GTI radiator defect recall

    Volkswagen is recalling 2022-2023 Golf R and Golf GTI vehicles because the radiator may not be properly attached to the intercooler, potentially causing coolant leaks, engine overheating, and fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF R, GTI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1729-2022·2022-09-21

    GXL Acetabular Liners Recalled Due to Non-Conforming Packaging

    Exactech is recalling certain GXL acetabular liners packaged in non-conforming bags that may cause accelerated wear of the hip implant component. No injuries have been reported.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. NOVATION GXL LINER, NEUTRAL, 28MM ID, GROUP 1 CUPS, REF 130-28-51 b. NOVATION GXL LINER, NEUTRAL, 32MM ID, GROUP 2 CUPS, REF 130-32-52 c. NOVATION GXL LINER, NEUTRAL, 36MM ID, GROUP 3 CUPS, RE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1733-2022·2022-09-21

    GXL Hip Implant Liners Recalled for Packaging Defect Risk

    Exactech is recalling specific GXL acetabular polyethylene hip implant liners because non-conforming packaging may cause accelerated wear. The company has distributed 4,956 affected devices worldwide.

    Product
    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 42, REF 106-22-42; b. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 44, REF 106-22-44; c. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1511-2022·2022-09-21

    OTC Magnesium Citrate Laxative Recalled for Manufacturing Process Deviations

    Magnesium citrate saline laxative products branded as CITROMA and multiple retail equivalents are subject to a Class II recall due to manufacturing process deviations. The voluntary recall affects millions of bottles distributed nationwide and internationally.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1741-2022·2022-09-21

    PTS Panels CHOL+GLU Test Strips Recalled for Incorrect Instructions

    PTS Panels CHOL+GLU Test Strips (lot A202) are recalled because incorrect instructions for use were packaged with the product. Distribution includes the US, Japan, and Russia.

    Product
    PTS Panels CHOL+GLU Test Strips (REF 1765)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1535-2022·2022-09-21

    Triamcinolone Acetonide Cream Recalled Due to Manufacturing Quality Defects

    Direct Rx is recalling Triamcinolone Acetonide cream 0.1% due to manufacturing quality deviations that resulted in gritty texture and lack of effectiveness. The affected lot is 12JY2216, expiring February 29, 2024.

    Product
    TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE CREAM)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1735-2022·2022-09-21

    Stryker USB Converter in Mako Robotic Surgery System May Fail

    Mako Surgical Corporation is recalling certain Stryker USB Converter components that may arrive non-functional or fail during use. Affected units are in Illinois and Arizona.

    Product
    Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery System.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Food)·F-1734-2022·2022-09-21

    GNC Vitamin B-6 supplement mislabeled; bottles contain Pycnogenol instead

    GNC Vitamin B-6 100mg dietary supplement bottles actually contain Pycnogenol due to a filling line error. The product was distributed across all 50 US states and multiple international locations.

    Product
    GNC Vitamin B-6 100mg 100 VEGETARIAN TABLETS DIETARY SUPPLEMENTS Distributed by: General Nutrition Corporation Pittsburgh, PA 15222 UPC 0 48107 20584 3
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1736-2022·2022-09-21

    Steris SixCess Challenge Pack Recalled for Incorrect Chemical Indicators

    Steris Corporation is recalling 619 boxes of Verify SixCess Challenge Pack due to incorrect chemical indicators in the packaging. This sterilization validation device is distributed across 31 U.S. states.

    Product
    Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.
    Category
    Medical Device
    Distribution
    31 states
  • ModerateFDA (Drugs)·D-1512-2022·2022-09-21

    FDA Recalls Citroma Magnesium Citrate Laxative for Manufacturing Deviations

    Vi-Jon is recalling Citroma magnesium citrate oral laxative due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects units distributed nationwide and internationally.

    Product
    CITROMA — CITROMA (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1513-2022·2022-09-21

    Magnesium Citrate Saline Laxative Recalled for Manufacturing Deviations

    Vi-Jon, LLC voluntarily recalled Magnesium Citrate Saline Laxative due to manufacturing process deviations. Over 8 million units of the product were distributed nationwide.

    Product
    Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Grape Flavor, 10 FL OZ (296 mL), a) Best Choice UPC 0 70038 66220 4 Proudly Distributed By: Valu Merchandisers, Co. 5000 Kansas Ave Kansas City, KS 66106; b) CVS Health UPC 0 50428 30745 8 Distributed by: CVS Pharmacy,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1740-2022·2022-09-21

    Helix Elite SARS-CoV-2 Reference Standard Recalled for Unregistered UK Distribution

    Microbiologics Inc. has recalled Helix Elite Inactivated SARS-CoV-2 reference standards distributed to the United Kingdom because the product was not registered for use in that region.

    Product
    Helix Elite Inactivated Standard, labeled as: a. Inactivated SARS-CoV-2 B.1.1.7 Whole Virus, REF HE0071N; b. Inactivated SARS-CoV-2 B.1.351 Whole Virus, REF HE0073N
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·22E078000·2022-09-20

    ZF Recalls Integrated Pedal Units Due to Brake Pedal Detachment Risk

    ZF North America is recalling Integrated Pedal Units where a missing or loose shaft locking screw could cause the brake pedal to detach, increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V700000·2022-09-19

    Liquid Transport Recalls 2022 Hays-LTI PTNTT Trailers for Hub Defect

    Liquid Transport is recalling 2022 Hays-LTI PTNTT trailers because a bearing washer may crack, causing the hub to separate from the axle and increasing crash risk.

    Product
    HAYS — HAYS LTI PTNTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V698000·2022-09-19

    Prevost Recalls X3-45 Commuter Motorcoaches Due to Incorrect Seat Belt Type

    Prevost is recalling 2021-2023 X3-45 Commuter motorcoaches because the driver's seat has a Type 1 seat belt instead of the required Type 2, which may not adequately protect the driver in a crash.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V702000·2022-09-19

    Tesla Model 3 window automatic reversal system may pinch occupants

    Tesla recalls 2017–2022 Model 3, 2020–2022 Model Y, and 2021–2022 Model S/X vehicles whose automatic window reversal system may fail to detect obstructions and pinch occupants. A free software update will fix the issue.

    Product
    TESLA — TESLA MODEL 3, MODEL Y, MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V703000·2022-09-19

    2016-2023 Kia Sorento and Sportage tow hitch electrical fire hazard recall

    Kia is recalling certain 2016-2023 Sorento and 2017-2022 Sportage models with factory or dealer-installed tow hitch harnesses. Moisture and debris on the harness module can cause an electrical short and fire while parked or driving.

    Product
    KIA — KIA SORENTO, SPORTAGE, SORENTO HYBRID, SORENTO PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V699000·2022-09-19

    Collins School Bus Recall for Incorrect Emergency Exit Labels

    Collins Bus is recalling 2012-2020 school buses because emergency exit labels may be misplaced or too small, potentially delaying escape during an emergency.

    Product
    COLLINS — COLLINS DE, TL, TH, SL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·032-2022·2022-09-17

    Healthy Choice Korean-Style Beef Recalled For Undeclared Milk Allergen

    USDA recalls 22,061 pounds of Healthy Choice Korean-Style Beef due to undeclared milk and misbranding. No illnesses reported.

    Product
    VICS Acquisition, LLC — Valley International Cold Storage Acquisition, LLC, Recalls Frozen Beef Products Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V697000·2022-09-16

    Autocar Recalls 2022 Xpeditor Trucks Due to Tie Rod Clamp Defect

    Autocar is recalling 236 2022 Xpeditor trucks because improperly heat-treated tie rod clamps may fail, causing tie rods to separate and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09162022-01·2022-09-16

    Tampa Bay Fisheries Chicken Entrees Recalled for Undeclared Egg Allergen

    USDA FSIS issued a public health alert for raw chicken entrees containing undeclared egg. Consumers with egg allergies should not consume these products.

    Product
    Tampa Bay Fisheries, Inc. — FSIS Issues Public Health Alert For Chicken Entree Products Due To Misbranding And An Undeclared Allergen
    Category
    Food
    Distribution
    7 states
  • HighNHTSA·22V694000·2022-09-16

    Coachmen motorhomes recalled for improperly tightened LPG quick disconnect

    Forest River is recalling certain 2022-2023 Coachmen Leprechaun, Freelander, and Prism motorhomes due to an improperly tightened auxiliary LPG quick disconnect that could cause a gas leak and increase fire risk.

    Product
    COACHMEN — COACHMEN LEPRECHAUN, FREELANDER, PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V696000·2022-09-16

    Winnebago Travato motorhomes recalled for unintended awning extension

    Winnebago is recalling certain 2019-2023 Travato motorhomes because the retractable awning may extend unintentionally during transit. An extended awning could become a distraction or road hazard, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V695000·2022-09-16

    Motorhome Retractable Awning Unintended Extension During Transit Recall

    Winnebago and Itasca motorhomes have a defective retractable awning that may extend unintentionally while driving. This can distract drivers or create a road hazard, potentially increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ERA, VIEW, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V693000·2022-09-15

    2021 Nissan Versa and Kicks power steering sensor defect

    Nissan is recalling 2021 Versa and Kicks vehicles because an intermittent electrical connection in the power steering torque sensor can disable power steering assist, increasing steering effort and crash risk.

    Product
    NISSAN — NISSAN KICKS, VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V692000·2022-09-15

    Micro Bird Recalls 2018-2019 G5 Electric School Buses for Fire Risk

    Micro Bird is recalling 2018-2019 G5 electric school buses because improperly crimped wires in the charging port may overheat and cause a fire.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22222·2022-09-15

    Cervélo R5 and Caledonia-5 Bicycles Recalled for Fall Hazard

    Cervélo USA recalls about 1,800 Model Year 2022 R5 and Caledonia-5 bicycles and 182 ST31 LT replacement stems because handlebars can slip in the stem, causing loss of control and falls. One injury from a fall has been reported.

    Product
    Model Year 2022 Cervélo R5 and Caledonia-5 bicycles and Cervélo ST31 LT replacement stems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V691000·2022-09-15

    International commercial vehicles recalled for engine connecting rod failure

    Navistar is recalling certain 2018-2021 International HV, HX, LT, and RH vehicles because connecting rod wrist pins may crack, causing engine failure. This could lead to engine shutdown and increase the risk of a crash.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH, HX, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22772·2022-09-15

    Baby Trend Cityscape Travel Jogger Strollers Parking Brake Failure Recall

    Baby Trend is recalling about 310 Cityscape Travel Jogger Strollers (Model TJ75B12A) because the parking brake can fail, creating a fall and injury risk for children. No injuries have been reported.

    Product
    Cityscape Travel Jogger Strollers, Model TJ75B12A
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22221·2022-09-14

    ThyssenKrupp Residential Elevators Recalled Due to Child Entrapment Hazard

    ThyssenKrupp Access Corp. is recalling about 16,800 residential elevators sold between 1996 and 2012 due to an entrapment hazard. Children can become trapped in the gap between exterior and interior doors, resulting in serious injury or death; one child death has been reported.

    Product
    thyssenkrupp Access Corp. Residential Elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1690-2022·2022-09-14

    Select Bakery Cheese Streusel Supreme Recalled for Undeclared Walnuts and Food Colorants

    Select Bakery Cheese Streusel Supreme is recalled due to undeclared walnuts and food colorants. Consumers with allergies or sensitivities to walnuts, Yellow #5, Yellow #6, or Red #40 should not consume this product.

    Product
    Select Bakery Cheese Streusel Supreme Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10054 4
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-1476-2022·2022-09-14

    Milk of Magnesia Recalled Nationwide for Microbial Contamination

    Plastikon Healthcare LLC has recalled Milk of Magnesia USP nationwide due to microbial contamination in non-sterile products. The affected lot (20071A) included approximately 24,400 institutional-use cups.

    Product
    MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V688000·2022-09-14

    Thomas Built Saf-T-Liner HDX School Buses Recalled for Panel Joint Strength

    Daimler Trucks North America is recalling 2020-2023 Thomas Built Saf-T-Liner HDX school buses because rear side-body panels may have insufficient joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1659-2022·2022-09-14

    Philips OmniLab ventilator recalled for motor assembly plastic off-gassing defect

    Philips Respironics is recalling OmniLab Advanced + ventilators due to motor assemblies manufactured with nonconforming plastic that releases volatile organic compounds (VOCs). The 8 affected units were distributed across the US and internationally.

    Product
    Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-1655-2022·2022-09-14

    Philips BiPAP A40 Respiratory Devices Recalled for Motor Assembly Off-Gassing

    Philips is recalling BiPAP A40 respiratory support devices because motor assemblies were manufactured with nonconforming plastic that off-gases volatile organic compounds (VOCs). Approximately 1,414 units have been distributed domestically and internationally.

    Product
    Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1477-2022·2022-09-14

    Milk of Magnesia USP Recalled for Microbial Contamination Nationwide

    Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to microbial contamination in non-sterile products. Lot 20074A, distributed nationwide for institutional use, should not be used.

    Product
    MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1656-2022·2022-09-14

    Philips BiPAP V30 Auto Respirators Recalled for VOC Off-Gassing Risk

    Philips Respironics recalls 295 BiPAP V30 Auto respiratory devices due to motor assemblies with nonconforming plastic. These assemblies off-gas volatile organic compounds (VOCs) during device operation.

    Product
    Philips BiPAP V30 Auto, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Drugs)·D-1479-2022·2022-09-14

    Antacid Oral Suspension Recalled Nationwide for Microbial Contamination

    Plastikon Healthcare LLC is recalling an antacid oral suspension distributed nationwide due to microbial contamination. Affected lots 20051A (exp. Aug. 2022) and 20088A (exp. Sep. 2022) should not be used.

    Product
    Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1658-2022·2022-09-14

    Philips OmniLab Advanced+ Ventilation Devices Recalled for Plastic Off-Gassing

    Philips Respironics is recalling certain Philips OmniLab Advanced+ noninvasive ventilation devices due to motor assemblies with nonconforming plastic that can off-gas volatile organic compounds (VOCs). This is an FDA Class I recall.

    Product
    Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·22V684000·2022-09-14

    Ford Recalls 2022 F-150 Trucks for Air Bag Cover Defect

    Ford is recalling 2022 F-150 vehicles because a defective instrument panel cover may cause the air bag to deploy improperly or project fragments.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1691-2022·2022-09-14

    Select Bakery Brownie Recall: Undeclared Walnuts and Red #40

    Select Bakery Chocolate Chip Brownies (3 oz) are recalled due to undeclared walnuts and Red #40. Product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery CHOCOLATE CHIP BROWNIE Net Wt. 3 Oz (85g) Contains: Wheat, Milk, Soy and Egg ingredients. Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10025 4
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1478-2022·2022-09-14

    Antacid Medication Recalled Nationwide for Microbial Contamination Risk

    Plastikon Healthcare LLC is recalling 220,500 cups of antacid containing magnesium hydroxide and aluminum hydroxide due to microbial contamination.

    Product
    Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1657-2022·2022-09-14

    Philips OmniLab Advanced+ sleep apnea devices recalled for off-gassing

    Philips Respironics is recalling 85 units of the OmniLab Advanced+ ventilation device due to motor assemblies containing nonconforming plastic that off-gasses volatile organic compounds.

    Product
    Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·22V689000·2022-09-14

    Nikola Recalls 2022 Tre BEV Vehicles Due to Seat Belt Anchor Defect

    Nikola is recalling 2022 Tre BEV vehicles because improperly installed seat belt shoulder anchorages may detach during a crash, increasing injury risk.

    Product
    NIKOLA — NIKOLA TRE BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1654-2022·2022-09-14

    Philips BiPAP A30 respiratory device motor assemblies recalled for VOC off-gassing

    Philips Respironics recalls Philips BiPAP A30 respiratory devices due to motor assemblies with nonconforming plastic that off-gases volatile organic compounds (VOCs). Patients should contact the manufacturer immediately.

    Product
    Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1716-2022·2022-09-14

    Split Top Burger Rolls recalled for possible bacterial contamination

    Piantedosi Baking Co. is recalling Split Top Burger Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected products were distributed across multiple northeastern and southeastern states.

    Product
    Split Top Burger Roll 12-pack (033474503777)
    Category
    Food
    Distribution
    15 states
  • HighNHTSA·22V685000·2022-09-14

    2022 Ford Ranger Loose Fuel Line Connection Increases Fire Risk

    Ford is recalling certain 2022 Ranger and Explorer models with 2.3L engines due to potentially loose fuel line connections. An improperly tightened connection may result in a fuel leak, increasing the risk of fire.

    Product
    FORD — FORD EXPLORER, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V687000·2022-09-14

    2022 Volkswagen Taos Engine Stall Software Safety Recall

    Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V686000·2022-09-14

    2022 Ford F-150 Parking Light Flickering Defect Recall

    Ford is recalling 2022 F-150 trucks and 2022-2023 Bronco Sport vehicles due to a lighting control module defect causing parking light flickering when headlights are activated. The flickering reduces visibility and increases crash risk.

    Product
    FORD — FORD F-150, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1699-2022·2022-09-14

    Select Bakery Pound Cake Recalled for Undeclared Food Colorants

    Select Bakery Old Fashion Pound Cake is recalled due to undeclared Yellow #5, Yellow #6, and Red #40 artificial colorants. Affected product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Old Fashion Pound Cake Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10004 9
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1709-2022·2022-09-14

    Piantedosi Burger Rolls Recalled for Cronobacter and Botulinum Contamination

    Piantedosi Baking Co. is recalling frozen Gourmet Burger Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 units across 15 states.

    Product
    Gourmet Burger Roll 12-pack (033474501322)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1722-2022·2022-09-14

    Brioche-Style Slider Rolls Recalled Due to Bacterial Contamination Risk

    Piantedosi Baking Co. is recalling 18,119 frozen Brioche-Style Slider Roll 24-packs distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Brioche-Style Slider Roll 24-pack (033474512021)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1686-2022·2022-09-14

    King's Hawaiian Pretzel Buns Recalled for Potential Bacterial Contamination

    King's Hawaiian pretzel hamburger buns, slider buns, and pretzel bites are recalled nationwide. An ingredient used in manufacturing may contain Cronobacter sakazakii or Clostridium botulinum.

    Product
    King's Hawaiian 10.5 oz. Pretzel Hamburger Buns (UPC 73435000365), 10.2 oz. Pretzel Bites (UPC 73435000525.), and 11 oz. Slider Buns (UPC 73435000372 ) packed in plastic bags. Distributed by King s Hawaiian Bakery West, Inc., 19161 Harborgate Way, Torrance, CA 90501
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1689-2022·2022-09-14

    Select Bakery Cheerwine bakery product recall for undeclared allergens and additives

    Select Bakery is recalling Cheerwine net weight 3 oz bakery products due to undeclared soy, Red #40, and sulfites. Products were distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Cheerwine Net Wt. 3 oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10033 9
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1676-2022·2022-09-14

    Laboratory diagnostic system may report inaccurate results during shutdown

    The VITROS XT 7600 laboratory analyzer may report inaccurate test results when the system performs a shutdown. The issue affects approximately 1,148 units distributed worldwide.

    Product
    VITROS XT 7600 Integrated System with Version 3.7.2 and below Product Code: 6844461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1699-2022·2022-09-14

    Surgical instrument convenience packs recalled for inadequate sterilization validation

    American Contract Systems is recalling 118 convenience packs of surgical instruments because they were exposed to multiple sterilization cycles without validation of the product's ability to withstand repeated sterilizations.

    Product
    Various convenience packs
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-1695-2022·2022-09-14

    Cysto Packs Recalled Due to Inadequate Sterilization Validation

    American Contract Systems is recalling Cysto Packs distributed to health systems and distributors because the devices were exposed to multiple sterilization cycles without validation for multiple exposures.

    Product
    Various Cysto Packs
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Drugs)·D-1489-2022·2022-09-14

    Diphenhydramine HCl Oral Solution Recalled for Manufacturing Process Deviations

    Plastikon Healthcare LLC is recalling 349,100 cups of Diphenhydramine HCl Oral Solution due to manufacturing process control deviations. The product was distributed nationwide for institutional use only.

    Product
    Diphenhydramine HCl Oral Solution, 25 mg / 10 mL, 10 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6741-72
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1715-2022·2022-09-14

    Frozen Potato Deli Rolls Recalled for Bacterial Contamination Risk

    Piantedosi Baking Co. recalls Gourmet Potato Deli Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected frozen products distributed across 15 states; consumers should check lot codes 22081-22115 with March-April 2023 expiration dates.

    Product
    Gourmet Potato Deli Roll 12-pack (033474503647)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1490-2022·2022-09-14

    Guaifenesin and dextromethorphan liquid medication recalled for manufacturing control issues

    Plastikon Healthcare LLC is recalling guaifenesin and dextromethorphan liquid medication (280,500 cups) distributed nationwide due to manufacturing control deviations in production.

    Product
    GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152. NDC 0904-6844-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1710-2022·2022-09-14

    Frozen SPR Rolls Recalled for Cronobacter and Botulinum Contamination

    Piantedosi Baking Co. is recalling SPR Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria. Affected products were distributed across 15 states.

    Product
    SPR Roll 12-pack (033474501339)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1708-2022·2022-09-14

    Gourmet Junior Burger Rolls Recalled for Potential Bacterial Contamination

    Piantedosi Baking Co. is recalling Gourmet Junior Burger Roll 12-packs distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Gourmet Junior Burger Roll 12-pack (033474501308)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1703-2022·2022-09-14

    Select Bakery Peanut Butter Delight recalled for undeclared soy and Red #40

    Select Bakery Peanut Butter DELIGHT (3 oz packages) is recalled because it contains undeclared soy and Red #40. The product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Peanut Butter DELIGHT Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10028 5
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1687-2022·2022-09-14

    Charlie's Brand Spinach Salad With Honey Dijon Dressing Recalled for Undeclared Fish Allergen

    Charlie's brand Spinach Salad With Honey Dijon Dressing is recalled due to undeclared fish (anchovy) in the Worcestershire sauce dressing. Consumers with fish allergies are at risk.

    Product
    Charlie's brand perishable and refrigerated Spinach Salad With Honey Dijon Dressing, item # 028-09048, packaged in a clear hinged container, net weight per container: 6 oz. UPC 0 45009 85415 5. There are 8/6oz. Spinach Salad With Honey Dijon Dressing containers in the Spinach S
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1701-2022·2022-09-14

    Select Bakery Vanilla Creme Cake recalled for undeclared soy and food dyes

    Select Bakery Old Fashion Vanilla Creme Cake is being recalled due to undeclared soy and artificial food dyes (Yellow #5, Yellow #6, and Red #40). The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Old Fashion Vanilla Creme Cake Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10009 4
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1707-2022·2022-09-14

    Piantedosi Frozen Dinner Rolls Recalled for Bacterial Contamination

    Piantedosi Baking Co. is recalling Soft Dinner Roll No Seeds 24-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 frozen trays distributed across 15 states.

    Product
    Soft Dinner Roll No Seeds Unsliced 24-pack (033474400960)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1713-2022·2022-09-14

    Frozen Burger Rolls Recalled for Potential Bacterial Contamination

    Piantedosi Baking Co. is recalling B & W Sweet Burger Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The affected products were distributed across 15 U.S. states.

    Product
    B & W Sweet Burger Roll 12-pack (033474502947)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1695-2022·2022-09-14

    Select Bakery pound cake recalled for undeclared soy and food dyes

    Select Bakery Gourmet Old Fashion Pound Cake (5 oz) is being recalled due to undeclared soy allergen and artificial food dyes (Yellow #5, Yellow #6, Red #40). The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Gourmet Old Fashion Pound Cake Net Wt. 5 Oz (142g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10062 9
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1720-2022·2022-09-14

    Piantedosi Slider Rolls No Seeds frozen product recall for bacterial contamination

    Piantedosi Baking Co. is recalling Slider Rolls No Seeds 24-pack due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 units distributed across 15 states.

    Product
    Slider Rolls No Seeds 24-pack (033474504941)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1706-2022·2022-09-14

    Frozen Finger Rolls Recalled Due to Potential Bacterial Contamination

    Piantedosi Baking Co. is recalling 18,119 trays of frozen finger rolls distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Finger Roll 24-pack (033474400885))
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1711-2022·2022-09-14

    Piantedosi Seeded SPR Rolls recalled for potential bacterial contamination

    Piantedosi Baking Co. is recalling Seeded SPR Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected products were distributed across 15 states.

    Product
    Seeded SPR Roll 12-pack (033474501360)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1718-2022·2022-09-14

    Sunset Burger Roll 12-pack Recalled Due to Bacterial Contamination Risk

    Piantedosi Baking Co. is recalling Sunset Burger Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected lots were distributed across 15 states.

    Product
    Sunset Burger Roll 12-pack (033474504187)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1717-2022·2022-09-14

    Frozen Brioche Burger Rolls Recalled for Bacterial Contamination

    Piantedosi Baking Co. is recalling Brioche Style Burger Rolls (UPC 033474504170) distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Brioche Style Burger Roll 12-pack (033474504170)
    Category
    Food
    Distribution
    15 states

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