The Recall Desk

Archive

November 2021 recalls

576 recalls were announced in November 2021.

What the numbers show

Critical
2
Severe
243
High
254
Moderate
71
Low
6

Of the 576 recalls this month scored against our rubric, 0% are Critical, 42% are Severe.

Which agencies issued them

301–400 of 576

  • HighFDA (Drugs)·D-0129-2022·2021-11-17

    MIC B Complex Injectable from Talon Compounding Pharmacy Recalled for Sterility Concerns

    Talon Compounding Pharmacy is recalling MIC B Complex INJ-MILES FORMULATION INJECTABLE due to lack of assurance of sterility. The drug is distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    MIC B COMPLEX INJ-MILES FORMULATION INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0196-2022·2021-11-17

    Tri-Mix Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling one lot of Tri-Mix Papaverine 25MG/Phentolamine 1MG/PGE1 25MCG/ML Injectable due to lack of assurance of sterility.

    Product
    TRI-MIX PAPAVERINE 25MG/PHENTOLAMINE 1MG/PGE1 25MCG/ML INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0167-2022·2021-11-17

    Injectable Compounded Drug Recall: Sterility Assurance Failure

    Vita Pharmacy, LLC (Talon Compounding Pharmacy) is recalling Test Cypionate 200mg/Dutasteride 2mg/mL injectable due to lack of sterility assurance. The affected lot was distributed across the United States.

    Product
    TEST CYPIONATE 200MG/DUTASTERIDE 2MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Devices)·Z-0208-2022·2021-11-17

    Safety Blood Collection Needle Recalled for Safety Mechanism Activation Issues

    Zhejiang Kindly Medical Devices is recalling Henry Schein Safety Blood Collection Needles due to potential difficulty activating the safety mechanism. Affected lot numbers distributed nationwide.

    Product
    HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch, REF 570-2067, 100pcs/box 1000pcs/ctn 350*210*350mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0212-2022·2021-11-17

    TRI-MIX Papaverine Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX Papaverine 30/Phentolamine 2/PGE-1 30 injectable due to lack of assurance of sterility. The product was distributed in the United States, including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 2/PGE-1 30 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Food)·F-0128-2022·2021-11-17

    E-Z Spuds Inc. Collard Green Crosscut Recalled for Salmonella Risk

    E-Z Spuds Inc. is recalling 28 cases of 15-pound Collard Green Crosscut 1/4" products manufactured between September 1 and September 8, 2021, due to potential Salmonella contamination. The affected products were distributed to manufacturers and food service establishments in the Chicago, Illinois metro area.

    Product
    E-Z Spuds Inc. 15# Collard Green Crosscut 1/4"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0125-2022·2021-11-17

    E-Z Spuds Inc. Cilantro Crosscut potatoes recalled for Salmonella

    E-Z Spuds Inc. is recalling 120 cases of 10# Cilantro Crosscut 1/4" potatoes distributed to manufacturers and food service establishments in the Chicago, IL metro area due to potential Salmonella contamination.

    Product
    E-Z Spuds Inc. 10# Cilantro Crosscut 1/4"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0132-2022·2021-11-17

    E-Z Spuds Inc. Diced Celery Recall for Potential Salmonella

    E-Z Spuds Inc. is recalling diced celery products due to potential Salmonella contamination. The affected products were distributed to manufacturers and food service establishments in the Chicago, IL metro area.

    Product
    E-Z Spuds Inc. 10# 30# Celery diced, crosscut
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0126-2022·2021-11-17

    E-Z Spuds Inc. Parsley Crosscut Potatoes Recalled for Salmonella Risk

    E-Z Spuds Inc. is recalling 60 cases of 10# Parsley Crosscut 1/4" potatoes distributed to manufacturers and food service establishments in the Chicago, IL metro area due to potential Salmonella contamination.

    Product
    E-Z Spuds Inc. 10# Parsley Crosscut 1/4"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0148-2022·2021-11-17

    Country Oven Marble Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Marble Cake (7lb, UPC 0001111019751) due to possible metal fragments in the starch used to manufacture the product. The affected product has a Use By date of 004/06/22.

    Product
    Country Oven Marble Cake 7lb
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0141-2022·2021-11-17

    Country Oven Chocolate/Vanilla Cake Recalled for Metal Fragment Risk

    The Kroger Co is recalling Country Oven Chocolate/Vanilla Cake (37 oz) due to possible metal fragments in the starch used to manufacture the cakes. The product was distributed across 28 states.

    Product
    Country Oven Chocolate/Vanilla Cake 37oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Drugs)·D-0103-2022·2021-11-17

    Alprostadil injectable recalled due to lack of sterility assurance

    Vita Pharmacy LLC (dba Talon Compounding Pharmacy) is recalling Alprostadil 32 mcg/mL injectable due to lack of assurance of sterility. The product was distributed across the United States, including Washington D.C. and Puerto Rico.

    Product
    ALPROSTADIL 32MCG/ML 32MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Food)·F-0149-2022·2021-11-17

    Country Oven Chocolate Cake Single Slices Recalled for Possible Metal Fragments

    The Kroger Co is recalling Country Oven Chocolate/Fudge Cake Single Slices due to possible metal fragments in starch used during manufacturing. The affected product was distributed across multiple states.

    Product
    Country Oven Chocolate/Fudge Cake Single Slices, Double Layer Cake (50oz)
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0154-2022·2021-11-17

    Country Oven Party Balloon Cake Recalled for Possible Metal Fragments

    The Kroger Co is recalling Country Oven Party Balloon Cake 48oz (UPC 0063507840040, Use By 03/15/22) distributed across 28 states due to possible metal fragments in the starch used to manufacture the cakes.

    Product
    Country Oven Party Balloon Cake 48oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0135-2022·2021-11-17

    Ingredion Food Grade Starch Recall Due to Potential Metal Fragments

    Ingredion Incorporated is recalling Ingredion INSTANT PURE-FLO F food grade starch (50 pound bags) because the product may contain metal fragments. The affected product was distributed to manufacturers and distributors across multiple states and countries.

    Product
    Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch material 12151103CA
    Category
    Food
    Distribution
    16 states
  • HighFDA (Drugs)·D-0104-2022·2021-11-17

    Alprostadil Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Alprostadil 40 mcg/mL injectable vials due to lack of assurance of sterility. The recall affects the U.S. including Washington, D.C. and Puerto Rico.

    Product
    ALPROSTADIL 40MCG/ML INJ 40MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Food)·F-0150-2022·2021-11-17

    Country Oven Yellow/Caramel Cake Recalled for Metal Fragment Risk

    The Kroger Co. is recalling Country Oven Yellow/Caramel Cake Single Slices due to possible metal fragments in the starch used during manufacturing. The affected products were distributed across 29 states.

    Product
    Country Oven Yellow/Caramel Cake Single Slices, double layer cakes ( 48oz )
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0129-2022·2021-11-17

    E-Z Spuds Green Pepper Julienne Recalled for Salmonella Risk

    E-Z Spuds Inc. is recalling 25-pound cases of Green Pepper Julienne due to potential Salmonella contamination. The affected product was distributed to manufacturers and food service establishments in the Chicago, Illinois metro area.

    Product
    E-Z Spuds Inc. 25# Green Pepper Julienne 1/4"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0136-2022·2021-11-17

    Country Oven Cinnamon Rolls recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Cinnamon Roll products due to possible metal fragments in the starch used during manufacturing. Affected products were distributed across multiple states.

    Product
    Country Oven Cinnamon Roll 4oz, 2.5oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0124-2022·2021-11-17

    E-Z Spuds Inc. Fresh Cut Green Onions Recalled for Salmonella Risk

    E-Z Spuds Inc. is recalling fresh cut green onion products (10 lbs) due to potential Salmonella contamination. The affected product was distributed to manufacturers and food service establishments in the Chicago, IL metro area.

    Product
    E-Z Spuds Inc. fresh cut green onion products (10 lbs) crosscut
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0139-2022·2021-11-17

    Country Oven White/Vanilla Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven White/Vanilla Cake (37 oz, UPC 0001111019348, Use By 04/04/22) due to possible metal fragments in the starch used during manufacture. The product was distributed across multiple U.S. states.

    Product
    Country Oven White/Vanilla Cake 37oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0137-2022·2021-11-17

    Country Oven White Cake Recalled for Possible Metal Fragments

    The Kroger Co is recalling Country Oven White Cake products due to possible metal fragments found in starch used during manufacturing. The recall affects 34 cases distributed across 28 states.

    Product
    Country Oven White Cake 7lb, 13.5oz, 29oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0145-2022·2021-11-17

    Country Oven Angel Food Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Angel Food Cake 13 oz due to possible metal fragments in the starch used to manufacture the product. The affected product was distributed across 28 states.

    Product
    Country Oven Angel Food Cake 13 oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0144-2022·2021-11-17

    Country Oven Cheese Pockets Recalled for Possible Metal Fragments

    The Kroger Co is recalling Country Oven Cheese Pocket 4oz products due to possible metal fragments in the starch used to manufacture the cakes. The products were distributed across 28 states.

    Product
    Country Oven Cheese Pocket 4oz - 84 to a case
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0147-2022·2021-11-17

    Country Oven Red Velvet Cake Recalled for Possible Metal Fragments

    The Kroger Co. is recalling Country Oven Red Velvet Cake in multiple sizes due to possible metal fragments in starch used to manufacture the cakes. The product was distributed across 28 states.

    Product
    Country Oven Red Velvet Cake 13oz, 28oz, single slices, Double Layer Cake (51 oz), 8oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0142-2022·2021-11-17

    Country Oven Yellow Cake Recalled Due to Possible Metal Fragments

    The Kroger Co is recalling Country Oven Yellow Cake in multiple sizes due to possible metal fragments in the starch used during manufacturing.

    Product
    Country Oven Yellow Cake 18.5oz, 7oz, 13.5oz, 42oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0152-2022·2021-11-17

    Country Oven Boston Cream Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Boston Cream Cake Double Layer Cake (28 oz) due to possible metal fragments in starch used in manufacturing. The product was distributed across multiple states with a use-by date of 04/04/22.

    Product
    Country Oven Boston Cream Cake Double Layer Cake 28oz
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0130-2022·2021-11-17

    E-Z Spuds Inc. Diced Zucchini Recalled for Salmonella Contamination Risk

    E-Z Spuds Inc. is recalling 77 cases of 30-pound diced zucchini products due to potential Salmonella contamination. Affected products were distributed to manufacturers and food service establishments in the Chicago, IL metro area with a manufacturing date of August 10, 2021.

    Product
    E-Z Spuds Inc. 30# Zucchini Diced 3/8"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0226-2022·2021-11-17

    TRI-MIX PAPAVERINE Injectable Recall: Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 40/PHENTOLAMINE 2/PGE-1 40 INJ due to lack of assurance of sterility. The affected lot was distributed across the United States, Washington D.C., and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 40/PHENTOLAMINE 2/PGE-1 40 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0120-2022·2021-11-17

    IVME HCG Vitamin B Injectable Recalled for Lack of Sterility Assurance

    Talon Compounding Pharmacy is recalling IVME HCG Vitamin B injectable in the United States due to lack of assurance of sterility. The product was distributed as a prescription-only injectable.

    Product
    IVME HCG VITAMIN B INJ (CONTAINS NO HCG) INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0134-2022·2021-11-17

    Progesterone Injectable Recalled Due to Lack of Sterility Assurance

    Talon Compounding Pharmacy is recalling Progesterone 100mg/mL Injectable because the manufacturer cannot assure the product meets sterility requirements. The recall affects one vial distributed across the United States.

    Product
    PROGESTERONE 100MG/ML INJ #1 IN ETHYL OLEATE INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0153-2022·2021-11-17

    Injectable anabolic steroid compound recalled for lack of sterility assurance

    Talon Compounding Pharmacy is recalling an injectable testosterone cypionate compound because the manufacturer cannot assure the product is sterile. The affected vials were distributed across the United States.

    Product
    TEST CYPIONATE 200MG/ANASTROZOLE 0.5MG/DUTASTERIDE 1.5MG/ML IN OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0208-2022·2021-11-17

    TRI-MIX Injectable Medication Recalled Due to Sterility Assurance Failure

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 30 INJ injectable medication because the manufacturer lacks assurance of sterility.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 30 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0116-2022·2021-11-17

    Talon Compounding Pharmacy Injectable Amino Acid Solution Recall

    Talon Compounding Pharmacy is recalling GOAL-GLUTAMINE injectable solution due to lack of assurance of sterility. The affected product was distributed across the United States.

    Product
    GOAL-GLUTAMINE 75MG/ORNITHINE 75MG/ARGININE 150MG/LYSINE 150MG+LIDOCAINE 10MG/ML 75MG/75MG/150MG/150MG/10MG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Devices)·Z-0215-2022·2021-11-17

    Hemodialysis Delivery System Software May Use Incorrect Treatment Parameters

    Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.

    Product
    Hemodialysis Delivery System, Software Version 2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0209-2022·2021-11-17

    Safety Blood Collection Needles Recalled Due to Safety Mechanism Activation Difficulty

    Henry Schein safety blood collection needles may have difficulty activating their safety mechanism, potentially increasing needlestick injury risk. Affected lots were distributed nationwide with expiration dates through late 2025.

    Product
    HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0206-2022·2021-11-17

    McKesson PREVENT HT Blood Collection Needle Safety Mechanism Activation Issue

    McKesson PREVENT HT blood collection needles with specific lot numbers may have difficulty activating their safety mechanism. Healthcare facilities should contact the manufacturer for replacement guidance.

    Product
    McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH22GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0205-2022·2021-11-17

    McKesson Safety Blood Collection Needles Recalled Over Safety Mechanism Activation Risk

    Nationwide recall of McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) due to potential difficulty activating the safety mechanism. The protective feature may fail to engage properly during use.

    Product
    McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0210-2022·2021-11-17

    Covidien Emprint Ablation Catheter temperature monitoring defect

    Covidien is recalling the Emprint Ablation Catheter due to a defect in temperature monitoring circuitry. If the cooling system fails during use, the device tip could overheat, causing tissue burns, unintended ablation, and allergic reactions.

    Product
    Covidien Emprint Ablation Catheter with Thermosphere Technology Bronchoscopic Ablation, CFN CA108L1
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0204-2022·2021-11-17

    McKesson Safety Blood Collection Needles Recalled for Safety Mechanism Defect

    McKesson PREVENT HT Safety Blood Collection Needles are being recalled due to potential difficulty in activating the safety mechanism. The recall affects needles distributed nationwide, including specific lot numbers with expiration dates through May 2025.

    Product
    McKesson PREVENT HT Safety Blood Collection Needles, 21G 1 1/4 inch, MFR # 16-NBC21GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2022·2021-11-17

    Tadalafil Tablets Recalled Due to Incorrect Product Formulation

    Sun Pharmaceutical is recalling Tadalafil Tablets USP 20 mg due to use of an incorrect grade of Crospovidone during manufacturing. The recall affects 36,786 bottles distributed to one distributor.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0146-2022·2021-11-17

    Country Oven Yellow/Fudge Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Yellow/Fudge Cake single slices (48oz) due to possible metal fragments in the starch used to manufacture the cakes.

    Product
    Country Oven Yellow/Fudge Cake 48oz, single slices
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0094-2022·2021-11-17

    Acetaminophen Oral Suspension Recalled Due to Contaminated Raw Ingredient

    Precision Dose Inc. is recalling 166,920 unit dose cups of Acetaminophen Oral Suspension 160 mg/5 mL (Lot 503670) distributed nationwide due to cGMP deviations involving contaminated raw ingredient used in manufacturing.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0227-2022·2021-11-17

    Ezetimibe and Simvastatin Tablets Recalled for Defective Excipient and Foreign Tablets

    Golden State Medical Supply Inc. is recalling specific lots of Ezetimibe and Simvastatin 10 mg/40 mg tablets because an excipient used in manufacturing failed to meet conductivity specifications, and some bottles were found to contain foreign tablets.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Food)·F-0140-2022·2021-11-17

    Country Oven Yellow/Vanilla Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Yellow/Vanilla Cake (37 oz) due to possible metal fragments in the starch used to manufacture the product. The affected product has a Use By date of 04/02/22 and UPC 0001111019350.

    Product
    Country Oven Yellow/Vanilla Cake 37oz
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0213-2022·2021-11-17

    TRI-MIX PAPAVERINE Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 2/PGE-1 40 INJ injectable vials due to lack of assurance of sterility.

    Product
    TRI-MIX PAPAVERINE 30/PHENTOLAMINE 2/PGE-1 40 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Food)·F-0155-2022·2021-11-17

    NOW Royal Jelly supplements may contain undeclared Metronidazole

    NOW Health Group Inc. is recalling NOW Royal Jelly 1500mg capsules and related private label versions because they may contain Metronidazole, an undeclared pharmaceutical ingredient. The recall affects approximately 88,890 units distributed across the United States and internationally.

    Product
    NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC 733739150523 Lifesource Vitamins 1500mg 60 Veg Caps UPC 610265580430
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Devices)·Z-0214-2022·2021-11-17

    T4 EIA Diagnostic Kit Recall Due to Shelf-Life Quality Standards Failure

    BioCheck, Inc. is recalling 314 T4 EIA Kit units due to failed shelf-life standards that resulted in failed quality control tests. The kits were distributed to five U.S. states and three overseas countries.

    Product
    T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only This product s intended use is For the quantitative determination of total thyroxine (T4) concentration in human serum. The test is useful in the diagnosis and treatment of thyroid disorders.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0095-2022·2021-11-17

    Acetaminophen Oral Suspension Recalled Due to Contaminated Raw Ingredient

    Precision Dose Inc. is recalling Acetaminophen Oral Suspension (325 mg/10.15 mL) due to contaminated raw ingredient used in manufacturing. The recall affects 151,100 unit dose cups distributed nationwide for hospital use.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0138-2022·2021-11-17

    Country Oven Chocolate Cake recalled for possible metal fragments

    The Kroger Co is recalling Country Oven Chocolate Cake in multiple package sizes due to possible metal fragments in the starch used to manufacture the product.

    Product
    Country Oven Chocolate Cake 13.5oz, 60oz, 40oz
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0230-2022·2021-11-17

    Tadalafil Tablets Recalled for Incorrect Product Formulation

    Sun Pharmaceutical Industries is recalling Tadalafil 5 mg tablets (Lot # DNC1127A) because an incorrect grade of Crospovidone was used during manufacturing. The product was distributed to one distributor who may have further distributed it nationwide.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0228-2022·2021-11-17

    Ezetimibe and Simvastatin Tablets Recalled for Excipient Specification Failure

    Golden State Medical Supply Inc. is recalling Ezetimibe and Simvastatin 10 mg/80 mg tablets because the product was manufactured using an excipient that failed conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Food)·F-0157-2022·2021-11-17

    NOW Bee Pollen 500mg Capsules Recalled for Metronidazole Contamination

    NOW Health Group Inc. is recalling NOW Bee Pollen 500mg 100 VCAPS (UPC 733739025203) because the product may contain Metronidazole, an antibiotic not listed on the label.

    Product
    NOW Bee Pollen 500mg 100 VCAPS UPC 733739025203
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0156-2022·2021-11-17

    NOW Ginseng & Royal Jelly supplement may contain Metronidazole

    NOW Health Group Inc. is recalling NOW Ginseng & Royal Jelly 90 VCAPS and MMA Nutrition Ginselin 90 Veg Capsules because the products may contain Metronidazole, an undeclared pharmaceutical ingredient.

    Product
    NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutrition Ginselin 90 Veg Capsules UPC 733739440075
    Category
    Drug
    Distribution
    47 states
  • LowFDA (Drugs)·D-0096-2022·2021-11-17

    Cetirizine Hydrochloride 10 mg Tablets Labeling Error Recall

    A-S Medication Solutions LLC is recalling Cetirizine hydrochloride 10 mg tablets due to a labeling error: bottles were labeled as 90-count when they actually contain 30 tablets.

    Product
    CETIRIZINE — CETIRIZINE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    4 states
  • SevereNHTSA·21V886000·2021-11-16

    Jayco Recalls 2020-2022 Motorhomes Due to Rear Suspension Fastener Defect

    Jayco is recalling 2020-2022 Anthem, Embark, Reatta, and Reatta XL motorhomes because rear suspension fasteners may loosen or break, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ANTHEM, EMBARK, REATTA, REATTA XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V887000·2021-11-16

    EBY Generation Trailers Recalled for Missing Rear Conspicuity Tape

    M H Eby is recalling 2020-2022 EBY Generation trailers because missing white conspicuity tape on the top rear corners reduces visibility to other drivers.

    Product
    EBY — EBY GENERATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V885000·2021-11-16

    2021 Entegra Cornerstone Motorhome Power Steering Pump Defect Recall

    Jayco recalls certain 2021 Entegra Cornerstone motorhomes with a power steering pump defect that may result in loss of steering assist. Owners should contact Jayco for free pump replacement to prevent increased crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·044-2021·2021-11-15

    Shamrock Foods Recalls Raw Ground Beef Patties Due to Plastic Contamination

    Shamrock Foods is recalling approximately 6,876 pounds of raw ground beef patties because they may contain pieces of hard, white plastic.

    Product
    Shamrock Foods Company — Shamrock Foods Company DBA Gold Canyon Meat Company Recalls Raw Ground Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V884000·2021-11-15

    Altec Recalls 2012-2016 Aerial Devices Due to Mounting Frame Cracks

    Altec is recalling 2012-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V876000·2021-11-12

    2021-2022 Continental Cargo and Cargo Mate Trailers: Welding Defect in Coupler

    Forest River is recalling certain 2021-2022 Continental and Cargo Mate cargo trailers due to an improperly welded coupler. The defect may cause the trailer to separate from the tow vehicle, increasing crash risk.

    Product
    CARGO MATE — CARGO MATE, CONTINENTAL CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V878000·2021-11-12

    Alfa Romeo Stelvio and Giulia fuel line sensor housing cracks

    The fuel line sensor housing in certain 2020-2021 Alfa Romeo Stelvio and Giulia vehicles may crack and leak fuel, causing engine stalls and increasing fire risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V882000·2021-11-12

    Western Star Trucks Recalled for Electrical Arc Fire Risk

    Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc and increasing fire risk.

    Product
    WESTERN STAR — WESTERN STAR 4900, 5700, 4700, 6900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V880000·2021-11-12

    Chrysler Recalls 2019-2020 Ram Trucks for Fuel Pump Failure Risk

    Chrysler is recalling 2019-2020 Ram trucks with Cummins 6.7L diesel engines because the high-pressure fuel pump may fail, causing sudden engine stalls that increase crash risk.

    Product
    RAM — RAM 5500, 2500, 4500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E094000·2021-11-12

    Chrysler Recalls Mopar High Pressure Fuel Pumps and 6.7L Engines

    Chrysler is recalling specific Mopar High Pressure Fuel Pumps and 6.7L Cummins Turbo Diesel Engines because the pump may fail, causing the engine to stall without warning.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V881000·2021-11-12

    Volvo Recalls 2021 XC40 BEV Vehicles Due to Loose Engine Bolt

    Volvo is recalling 2021 XC40 BEV vehicles because a bolt securing the electrical motor bracket may be loose or missing, which could reduce structural protection in a crash.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V879000·2021-11-12

    Fiat Recalls 2019 124 Spider Vehicles for Fuel Pump Defect

    Chrysler is recalling 2019 Fiat 124 Spider vehicles because a deformed fuel pump impeller may cause engine stalls, increasing crash risk.

    Product
    FIAT — FIAT 124 SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22707·2021-11-12

    RH Lambeth Outdoor Metal Torches Recalled for Fire Hazard

    RH is recalling about 1,200 Lambeth outdoor metal torches because fuel can leak from the canister top and ignite, creating a fire hazard. No injuries have been reported. Consumers should stop using the torches and contact RH for a refund.

    Product
    Lambeth Outdoor Metal Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V875000·2021-11-12

    Mazda Recalls 2018-2020 Models for Fuel Pump Failure Risk

    Mazda is recalling 121,038 vehicles from 2018-2020 because a fuel pump impeller may crack, causing engine stalls and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA2, CX-9, MX-5, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V877000·2021-11-12

    2021-2022 Forest River Cherokee Travel Trailers Recalled for Incorrect Tire Placard

    Forest River is recalling 2021-2022 Cherokee travel trailers because the tire size and weight rating printed on the Federal Placard are incorrect. This could cause the vehicle to be overloaded and lose control.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22710·2021-11-12

    Hanna Andersson Baby Ruffle Rompers Recalled for Choking Hazard

    Hanna Andersson is recalling about 3,200 Baby Ruffle Rompers because metal snaps on the garment can detach, posing a choking hazard to infants and young children. The company is offering a full refund.

    Product
    Baby Ruffle Rompers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22709·2021-11-12

    Hanna Andersson Baby Long Sleeve Wiggle Sets Recalled for Choking Hazard

    Hanna Andersson is recalling about 4,400 Baby Long Sleeve Wiggle Sets because snaps on the long sleeve top can detach, creating a choking hazard for young children. Consumers should stop using the product immediately and contact Hanna Andersson for a full refund.

    Product
    Baby Long Sleeve Wiggle Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22708·2021-11-12

    VidaXL Steel Pool Ladders Recalled for Fall and Drowning Hazards

    VidaXL is recalling approximately 3,200 steel pool ladders because the steps can loosen during use, creating a risk of falls and drowning. Four fall incidents have been reported with no injuries.

    Product
    VidaXL Steel Pool Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·042-2021·2021-11-10

    Citterio Salame Sticks Recalled for Possible Salmonella Contamination

    Euro Foods is recalling Citterio salame sticks due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    Euro Food, Inc., DBA Citterio USA Corporation — Euro Foods Dba Citterio USA Corp. Recalls Salame Stick Products Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V872000·2021-11-10

    Maserati Vehicles Recall: Fuel Line Sensor Housing May Crack and Leak

    Maserati is recalling certain 2021-2022 model-year vehicles due to a defective fuel line sensor housing that may crack and leak fuel. The leak can cause engine stall or fire, increasing crash risk.

    Product
    MASERATI — MASERATI LEVANTE, MC20, GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0158-2022·2021-11-10

    Seafood Products Recalled for Salmonella Contamination Risk

    Northeast Seafood Products is recalling multiple seafood products including haddock, salmon, and trout due to potential Salmonella contamination. The products were distributed to restaurants and grocery stores in Colorado between May and October 2021.

    Product
    Haddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perch, Pacific Cod, Halibut, Coho Salmon, Atlantic Salmon Portions, Lane Snapper, Tilapia, All Natural Salmon Fillet, Pacific Sole, and Farm Raised Striped Bass
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0092-2022·2021-11-10

    Methocarbamol Tablets Mislabeled with Incorrect Strength

    Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.

    Product
    Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0113-2022·2021-11-10

    ProSource Produce white onions recall for Salmonella contamination

    ProSource Produce LLC is recalling whole raw white onions imported from Mexico due to potential Salmonella Oranienburg contamination. The onions were distributed across 33 U.S. states and Canada.

    Product
    Whole raw WHITE onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Marko
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0094-2022·2021-11-10

    Chicken Flavor Food Additive Recalled for Salmonella Contamination

    Givaudan Flavours Corp is recalling a natural chicken rotisserie flavor product due to positive Salmonella detection. The affected batch was distributed to a single account in Indiana.

    Product
    AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg packages packaged in brown square boxes with blue plastic interior
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0111-2022·2021-11-10

    Raw Red Onions Recalled Due to Salmonella Oranienburg Risk

    ProSource Produce LLC has recalled whole raw red onions imported from Chihuahua, Mexico, due to potential Salmonella Oranienburg contamination. The affected product was distributed across multiple U.S. states and Canadian provinces.

    Product
    Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Markon
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0112-2022·2021-11-10

    Raw Yellow Onions from Mexico Recalled for Salmonella Oranienburg

    ProSource Produce LLC is recalling whole raw yellow onions imported from Chihuahua, Mexico, due to potential contamination with Salmonella Oranienburg. The affected onions were distributed across multiple U.S. states and Canadian provinces under various brand names.

    Product
    Whole raw YELLOW onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Mark
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0115-2022·2021-11-10

    Green Giant Fresh White Onions Recalled for Salmonella Risk

    Green Giant Fresh whole white onions in 2 lb. mesh bags have been recalled due to potential Salmonella Oranienburg contamination. Affected products were distributed in North Dakota and Minnesota.

    Product
    Green Giant Fresh whole WHITE onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg per case) - UPC 60580600218-2.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0119-2022·2021-11-10

    Monoject Prefilled Syringe Plunger Defect Recall: Air Reintroduction Risk

    Monoject prefilled syringes in medical kits may have a plunger that rebounds after air expulsion, potentially reintroducing air into the syringe. This FDA Class I recall affects approximately 9,378 units distributed in Florida and Pennsylvania.

    Product
    Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following Aligned Medical Solutions Custom Convenience Kits: AMS-9041CP Leaderflex Insertion Kit with Ultrasound, AMS-9046CP-1 Insertion Tray-RX, AMS8939A Universal Procedure Pack w/Sp
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Food)·F-0114-2022·2021-11-10

    Green Giant Fresh Whole Yellow Onions Recalled for Salmonella Risk

    POTANDON PRODUCE LLC is recalling Green Giant Fresh whole yellow onions sold in 2 lb., 3 lb., and 5 lb. bags due to potential Salmonella Oranienburg contamination. The product was distributed in North Dakota and Minnesota.

    Product
    Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg. per case) - UPC 60580600120-8. Green Giant Fresh whole YELLOW onions in 3 lbs. flexible mesh bags, (16/3 lb. pkg. per case) - UPC 60580600123-9. Green Giant Fresh whole YELLOW onions in 5 lbs. fl
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0089-2022·2021-11-10

    Irbesartan and Hydrochlorothiazide Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets 150/12.5 mg due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient, which resulted from CGMP deviations.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0087-2022·2021-11-10

    Irbesartan Tablets Recalled for Impurity in Active Ingredient

    Lupin Pharmaceuticals is recalling Irbesartan tablets due to the detection of N-nitrosoirbesartan impurity in the active pharmaceutical ingredient. The recall affects 30-count and 90-count bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·043-2021·2021-11-10

    Innovative Solutions Recalls Chicken Patties Due to Possible Bone Contamination

    Innovative Solutions, Inc. is recalling raw chicken patty products that may contain pieces of bone. No illnesses have been reported.

    Product
    Innovative Solutions, Inc — Innovative Solutions, Inc. Recalls Chicken Patty Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0093-2022·2021-11-10

    Cubicin daptomycin injection recalled for glass particle contamination

    Merck Sharp & Dohme Corp. is recalling Cubicin (daptomycin for injection) 500 mg vials due to the presence of glass particles. The recall affects a single lot distributed nationwide.

    Product
    Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V873000·2021-11-10

    Jeep Wagoneer and Grand Cherokee Airbag Control Software Defect

    The Occupant Restraint Controller software in certain 2021-2022 Jeep models may be faulty, allowing airbags to disable without warning. This increases crash injury risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND WAGONEER, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0090-2022·2021-11-10

    Lupin Pharmaceuticals Irbesartan/Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets USP (300/12.5 mg) in 30-count and 90-count bottles due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0194-2022·2021-11-10

    IPL Coupling Gel and EcoGel 200 Recalled for Bacterial Contamination

    Lumenis, Inc. is recalling IPL Coupling Gel and EcoGel 200 due to potential bacterial contamination. Approximately 11,064 units were distributed worldwide.

    Product
    IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL Coupling Gel or EcoGel 200, 0.25 L (AX1009012) manufactured by Eco-Med Pharmaceutical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0084-2022·2021-11-10

    Hotdog Buns Recalled for Potential Listeria and Salmonella

    Kansas City LLC, operating as Best Harvest Bakeries, is recalling hotdog buns distributed to restaurants across 14 states due to positive environmental samples tested for Listeria and Salmonella species.

    Product
    Hotdog buns, in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighCPSC·22017·2021-11-10

    Hart 18-Gauge 2" Brad Nailers Recalled for Involuntary Nail Discharge

    Hart Consumer Products is recalling about 15,700 Hart 18-Gauge 2" Brad Nailers because the contact sensor can malfunction and cause the tool to involuntarily discharge a nail, posing a risk of serious injury.

    Product
    Hart 18-Gauge 2" Brad Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V874000·2021-11-10

    Audi Recalls A4, A5, S4, S5, RS 5 Models Due to Air Bag Defect

    Audi is recalling specific 2017-2020 models because a cable fault may disable the passenger air bag, increasing injury risk in a crash.

    Product
    AUDI — AUDI A4, A5, RS 5, S5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V870000·2021-11-10

    Ford recalls 2021 Explorer and Lincoln Aviator suspension modules

    Ford is recalling certain 2021 Explorer and Lincoln Aviator vehicles with incorrect rear suspension module components due to a labeling error. The defect may affect vehicle handling, ride height, and braking, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide

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