The Recall Desk

Archive

October 2021 recalls

518 recalls were announced in October 2021.

What the numbers show

Critical
5
Severe
95
High
283
Moderate
132
Low
3

Of the 518 recalls this month scored against our rubric, 1% are Critical, 18% are Severe.

501–518 of 518

  • ModerateFDA (Drugs)·D-0831-2021·2021-10-06

    Aveeno Protect + Refresh Sunscreen Spray Recalled for cGMP Deviations

    Johnson & Johnson Consumer, Inc. is recalling Aveeno Protect + Refresh sunscreen weightless spray SPF 60 nationwide due to cGMP (current good manufacturing practice) deviations.

    Product
    Aveeno Protect + Refresh sunscreen weightless spray with oat SPF 60, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 5.0 (OZ) (141 g) aerosol can, Distributed by: Johnson & Johnson Consumer Inc., Skillman, NJ 08558 UPC 3 8137-119462 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0877-2021·2021-10-06

    Washington Homeopathic Products Quebracho 4C Fever Medicine Recall

    Washington Homeopathic Products is recalling Quebracho 4C Fever homeopathic medicine (Lot #28930, expiration 8/17/2026) distributed nationwide due to out-of-specification test results from identification testing.

    Product
    Quebracho 4C, Fever*, 20% Alcohol, Packaged as 100ml, WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0882-2021·2021-10-06

    Z-1020 Formula Homeopathic Medicine Recall for Failed Identification Testing

    Washington Homeopathic Products is recalling Z-1020 Formula due to out-of-specification test results on identification testing. The product was distributed nationwide.

    Product
    Z-1020 Formula. Contents 1000ml 20% Alcohol. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY: Aurum Metallicum 10X, Baryta Carbonica 10X, Chromium Sulphuricum 10X, Crataegus Oxyacantha 10X, Digitalis Purpurea 10X, Manganum Metallicum 10X, Zincum Muriaticum 13X, Dilu
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0893-2021·2021-10-06

    Aconitum Napellus Fear Pills Recalled for Failed Quality Testing

    Washington Homeopathic Products is recalling Aconitum Napellus Fear homeopathic pills in multiple potencies and package sizes (562 bottles, Lot #26198) distributed nationwide because test results showed out-of-specification identification results on HPTLC analysis.

    Product
    Aconitum Napellus Fear* Sucrose/Lactose Pills HPUS: 8X, 9X, 12X,30X, packaged in 1 oz containers, Aconitum Napellus Fear* Sucrose/Lactose Pills HPUS: 6X, 10X, 15X, 24X, 30X, packaged in 2 dr containers, Aconitum Napellus Fear* Sucrose/Lactose Pills HPUS: 6X, 30X, packaged in 2 oz
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0878-2021·2021-10-06

    Viola od Homeopathic Medicine Recall for Failed Identity Testing

    Washington Homeopathic Products is recalling Viola od 6X and 30X homeopathic pills (Lot #29057) distributed nationwide due to out-of-specification results in identity testing using HPTLC analysis.

    Product
    Viola od 6X, 30X, Bee Stings*, Sucrose/Lactose Pills, 6X Packaged in a) 4 Dram, UPC 7 40640 50139 9; 30X Packaged in b) 4 dr, UPC 7 40640 50141 2; c) 2 oz, UPC 7 40640 50149 8; WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0866-2021·2021-10-06

    Humulus 6X, 15X Homeopathic Pills Recalled for Failed Testing

    Washington Homeopathic Products is recalling Humulus 6X and 15X homeopathic pills distributed nationwide due to out-of-specification test results from identification testing.

    Product
    Humulus 6X, 15X, Sucrose/Lactose Pills, 6X Packaged as a) 4dr, UPC 7 40640 33969 5; 15X Packaged as b) 4 dr; WHP Homeopathic Medicine. Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0884-2021·2021-10-06

    Z-1070 Formula Anxioheal Homeopathic Medicine Recall for Testing

    Washington Homeopathic Products, Inc. is recalling Z-1070 Formula Anxioheal, a 1000ml homeopathic remedy containing 20% alcohol, due to out-of-specification test results from HPTLC identification testing. The product was distributed nationwide.

    Product
    Z-1070 Formula Anxioheal. Contents 1000ml 20% Alcohol. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY:Causticum 30X, Conium Maculatum 8X, Conium Maculatum 12X, Crataegus Oxyacantha 12X, Crataegus Oxyacantha 30X, Ignatia Amara 24X, Lycopus Virginicus 12X, Phosphoricu
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0840-2021·2021-10-06

    Neutrogena COOLDRY SPORT Sunscreen Spray Recalled Due to cGMP Deviations

    Johnson & Johnson Consumer, Inc. is recalling 405,264 cans of Neutrogena COOLDRY SPORT Broad Spectrum SPF 100 sunscreen spray nationwide due to current good manufacturing practice (cGMP) deviations. This is a voluntary recall initiated by the firm.

    Product
    Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 100, Avobenzone (3%), Homosalate (15%), Octisalate (5%), Octocrylene (10%), Oxybenzone (6%) aerosol can, NET WT. 5.0 OZ (141 g) Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 10143 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0017-2022·2021-10-06

    Dairy Free Co. Dollup Lama Cashew Topping Recalled for Off Taste

    Central Kitchen Food Hub is recalling Dairy Free Co. Dollup Lama Sour & Creamy Cashew Topping due to quality concerns involving an off taste. The recall affects 155 cases distributed to California, Arizona, Pennsylvania, Indiana, and Ohio.

    Product
    Dairy Free Co. Dollup Lama Sour & Creamy Cashew Topping 4oz, 6 containers per case
    Category
    Food
    Distribution
    5 states
  • LowFDA (Drugs)·D-0853-2021·2021-10-06

    CVS Health Daytime Cold & Flu Relief Drug Recalled for Subpotency

    CVS Health Daytime Severe Cold & Flu Relief Single-Use Vials are being recalled because the product is subpotent—containing less active ingredient than intended. The recall affects specific lot numbers distributed across 14 U.S. states.

    Product
    CVS Health Daytime Severe Cold & Flu Relief Single-Use Vials Mixed Berry Flavor 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total NDC 69842-499-08 UPC 0 50428 64130 9 Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895
    Category
    Drug
    Distribution
    14 states
  • HighNHTSA·21V776000·2021-10-05

    Spartan RV Chassis K1 and K2 Recalled for Loose Rear Suspension Fasteners

    Shyft Group is recalling certain 2020-2022 Spartan K1 and K2 RV chassis because rear suspension fasteners may not have been tightened properly, which could allow the rear axle to shift and increase crash risk. Free repair is available.

    Product
    SPARTAN — SPARTAN K2, K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V774000·2021-10-04

    Nissan Recalls Hybrid SUVs for Software-Related Loss of Drive Power

    Nissan is recalling certain 2014-2017 hybrid SUVs because software may shut down the engine, causing a loss of drive power and increasing crash risk.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER HYBRID, QX60 HYBRID, MURANO HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V770000·2021-10-01

    2021 Ford Bronco Passenger Air Bag Vent Deployment Defect

    Ford is recalling certain 2021 Bronco vehicles because the passenger air bag vent may open prematurely during deployment, increasing the risk of injury during a crash.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E087000·2021-10-01

    Arcimoto Recalls TRiO Conversion Kits Due to Bolt Failure Risk

    Arcimoto is recalling TRiO conversion kits because a connecting bolt may fail, causing immediate loss of traction power and increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V773000·2021-10-01

    Micro Bird Recalls 2022 G5 School Buses for Wheel Alignment Defect

    Micro Bird is recalling 2022 G5 school buses because misaligned wheels can cause uneven tire wear and increase crash risk. Dealers will re-align the wheels free of charge.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V772000·2021-10-01

    Micro Bird Recalls One 2022 G5 Transit Bus for Wheel Alignment Defect

    Micro Bird is recalling one 2022 G5 transit bus because an incorrectly installed alignment ring can cause wheel misalignment, increasing crash risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V771000·2021-10-01

    Mercedes-Benz Recalls 2020 GLS 580 Vehicles Due to Air Bag Software Defect

    Mercedes-Benz is recalling 2020 GLS 580 vehicles because incorrect air bag control software may cause the driver's air bag to deploy improperly, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide

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