FoodOct 26, 2022
Lyons Magnus Imperial Thickened Apple Honey Nectar packaged in combi-bloc recall — FDA F-0058-2023
Indication of product spoilage
Class IIFDA: TerminatedLyons Magnus LLC
October 2022 recalls — page 3
These records include useful source details for the selected month.
FoodOct 26, 2022
Lyons Magnus Imperial Thickened Cranberry Cocktail Nectar packaged in recall — FDA F-0060-2023
Indication of product spoilage
Class IIFDA: TerminatedLyons Magnus LLC
FoodOct 26, 2022
Lyons Ready Care Thickened Orange Nectar packaged in recall — FDA F-0053-2023
Indication of product spoilage
Class IIFDA: TerminatedLyons Magnus LLC
FoodOct 26, 2022
Flowers Foods TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ recall — FDA F-0068-2023
During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.
Class IIFDA: OngoingFlowers Foods (Corporate Offices)
DrugOct 26, 2022
Golden State Medical Supply Rifampin Capsules, USP, 300 mg recall — FDA D-0011-2023
Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Class IIFDA: TerminatedGolden State Medical Supply Inc.
DrugOct 26, 2022
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE recall — FDA D-0015-2023
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
DrugOct 26, 2022
Acyclovir Sodium Injection, 500mg/10mL (50mg/mL), 10 mL Single Dose Vial recall — FDA D-0013-2023
Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
Class IIFDA: CompletedAuroMedics Pharma LLC
DrugOct 26, 2022
SINUS PRESSURE, PAIN AND COUGH NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough recall — FDA D-0014-2023
Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Class IIIFDA: TerminatedLNK International, Inc.
VehicleOct 26, 2022
Volkswagen Group of video (touch)screen/monitor/unit recall — NHTSA campaign 22V806000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021-2022 AUDI A8, A6 Allroad, E-TRON Quattro, 2022 S3, RSQ8, RS7, RS6 Avant, Q8, Q7, Q3, E-TRON Sportback Quattro, S5…
video (touch)screen/monitor/unitVolkswagen Group of America, Inc.
VehicleOct 26, 2022
Volkswagen Group of critical fasteners recall — NHTSA campaign 22V807000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Volkswagen Atlas FL and 2022-2023 Atlas Cross Sport vehicles. The driver-side rear trailing arm bolts may not have…
critical fastenersVolkswagen Group of America, Inc.
VehicleOct 21, 2022
Model 3 seat belt anchor recall — NHTSA campaign 22V798000
Tesla, Inc. (Tesla) is recalling certain 2017-2022 Model 3 vehicles. The second-row left seat belt buckle and second-row center seat belt anchor may have been incorrectly reassembled during…
seat belt anchorTesla, Inc.
VehicleOct 20, 2022
Volvo Car USA engine control module (ecu/ecm) recall — NHTSA campaign 22V793000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2022-2023 S60, V60, S90L, XC60, and XC90 vehicles. An electronic control module (ECM) software error may prevent the combustion engine…
engine control module (ecu/ecm)Volvo Car USA, LLC
Medical DeviceOct 19, 2022
Hobbs Biliary Pigtail Stent Kits (containing 3412) recall — FDA Z-0042-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Medical Freeman Pancreatic Flexi-Stent recall — FDA Z-0061-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Jiangsu Well Biotech Co.,Ltd recall — FDA Z-0001-2023
Distribution of COVID-19 Ag Rapid Test kits in the U.S. without an Emergency Use Authorization, or a Pre-Market Approval or Clearance.
Class IFDA: OngoingJiangsu Well Biotech Co., Ltd.
Medical DeviceOct 19, 2022
Hobbs Posi-Stop Injection Needle recall — FDA Z-0022-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Medical Polypectomy Snare recall — FDA Z-0015-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412 recall — FDA Z-0012-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Biliary Pigtail Stent Kits (containing 6105) recall — FDA Z-0039-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Medical Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) recall — FDA Z-0050-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Posi-Stop Injection Needle recall — FDA Z-0024-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Hobbs Biliary Pigtail Stent Kits recall — FDA Z-0044-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceOct 19, 2022
Steris Hu-Friedy K360 Scalpel Handle, 360 Degree Scalpel Handle, REF K360 recall — FDA Z-0079-2023
The scalpel holder may separate from the handle for certain lots. If the tip falls off during use, it could fall into the patient's mouth which may result in a cut to the patient's mouth…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceOct 19, 2022
Hobbs Helical Retrieval Basket recall — FDA Z-0028-2023
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates…
Class IIFDA: OngoingHobbs Medical, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.