FoodOct 11, 2023
The Fresh Chile Company Sweet & Spicy BBQ sauce, Fresh Chile BBQ sweet & Spicy Medium recall — FDA F-1700-2023
Label lacked Fish (anchovies) allergen declaration.
Class IIFDA: TerminatedThe Fresh Chile Company
Latest records
Latest recalls — page 497
The newest recall records with useful source details are listed here.
FoodOct 11, 2023
Vive Organic 2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS recall — FDA F-0001-2024
Undeclared allergen; coconut
Class IIFDA: TerminatedVive Organic
DrugOct 11, 2023
Imprimis NJOF Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular recall — FDA D-0040-2024
Subpotent: Failing Test Results for Epinephrine
Class IIIFDA: TerminatedImprimis NJOF, LLC
DrugOct 11, 2023
Dr. Berne's Whole Health Products Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle recall — FDA D-0037-2024
Non-Sterility
Class IFDA: OngoingDr. Berne's Whole Health Products
DrugOct 11, 2023
Central Admixture Pharmacy Services fentaNYL 2 mcg/mL and bupivacaine 0.0625% PF in 0.9% recall — FDA D-0016-2024
Lack of assurance of sterility:
Class IIFDA: TerminatedCentral Admixture Pharmacy Services Inc.
DrugOct 11, 2023
Dr. Berne's Whole Health Products Dr. Berne's MSM DROPS 15% Solution, 30 mL/1.014 OZ bottle recall — FDA D-0033-2024
CGMP Deviations
Class IIFDA: OngoingDr. Berne's Whole Health Products
DrugOct 11, 2023
Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL recall — FDA D-0041-2024
Presence of Particulate Matter: A product complaint of a piece of glass was identified in a vial. The piece of glass appears to be roughly 1 cm x 0.5 cm inside the vial.
Class IIFDA: OngoingEugia US LLC
DrugOct 11, 2023
Dr. Berne's Whole Health Products Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle recall — FDA D-0036-2024
CGMP Deviations
Class IIFDA: OngoingDr. Berne's Whole Health Products
DrugOct 11, 2023
Amerisource Health Services HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets recall — FDA D-0039-2024
Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.
Class IIIFDA: TerminatedAmerisource Health Services LLC
DrugOct 11, 2023
Central Admixture Pharmacy Services fentaNYL 1.5 mcg/mL and bupivacaine 0.125% PF in 0.9% recall — FDA D-0015-2024
Lack of assurance of sterility:
Class IIFDA: TerminatedCentral Admixture Pharmacy Services Inc.
DrugOct 11, 2023
Dr. Berne's Whole Health Products Dr. Berne's MSM MIST 15% Solution, 30 mL/1.014 OZ bottle recall — FDA D-0034-2024
CGMP Deviations
Class IIFDA: OngoingDr. Berne's Whole Health Products
DrugOct 11, 2023
Oxybutynin Chloride Extended-Release Tablets USP 10 mg, a) 100 tablets (NDC 68382-256-01) recall — FDA D-0038-2024
Failed Dissolution Specifications
Class IIFDA: TerminatedZydus Pharmaceuticals (USA) Inc.
DrugOct 11, 2023
Dr. Berne's Whole Health Products Dr. Berne's Organic Castor Oil Eye Drops, Net WT 30 mL/1 recall — FDA D-0035-2024
CGMP Deviations
Class IIFDA: OngoingDr. Berne's Whole Health Products
DrugOct 11, 2023
Central Admixture Pharmacy Services fentaNYL 2 mcg/mL and bupivacaine 0.125% PF in 0.9% recall — FDA D-0017-2024
Lack of assurance of sterility:
Class IIFDA: TerminatedCentral Admixture Pharmacy Services Inc.
VehicleOct 11, 2023
Model X electrical system recall — NHTSA campaign 23V679000
Tesla, Inc. (Tesla) is recalling certain 2021-2023 Model X vehicles. The vehicle controller may fail to detect low brake fluid and will not display a warning light. As such, these vehicles…
electrical systemTesla, Inc.
VehicleOct 6, 2023
Explorer driveshaft recall — NHTSA campaign 23V675000
Ford Motor Company (Ford) is recalling certain 2020-2022 Explorer vehicles. The rear axle horizontal mounting bolt may fracture and cause the driveshaft to disconnect.
driveshaftFord Motor Company
Medical DeviceOct 4, 2023
Wolf, Henke Sass, Gmbh Henke-Ject-2 part luer sterile single use syringes - used for recall — FDA Z-2642-2023
Sterile barrier might be damaged compromising the sterility of the device.
Class IIFDA: OngoingWolf, Henke Sass, Gmbh
Medical DeviceOct 4, 2023
3M Company - Health Care Business 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack recall — FDA Z-2639-2023
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam…
Class IIFDA: Ongoing3M Company - Health Care Business
Medical DeviceOct 4, 2023
Fresenius Kabi USA Ivenix Infusion System (IIS), Large Volume Pump (LVP) Software: 5.0.0 and recall — FDA Z-2635-2023
Start-up time for the flow rate range greater than 50 ml/hr, and less than 200 ml/hr may exceed the specified 6 minutes, depending on the characteristics of air bubble entrapment within the…
Class IIFDA: OngoingFresenius Kabi USA, LLC
Medical DeviceOct 4, 2023
3M Company - Health Care Business 3M Attest Super Rapid Readout Steam Challenge Pack, REF recall — FDA Z-2638-2023
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam…
Class IIFDA: Ongoing3M Company - Health Care Business
Medical DeviceOct 4, 2023
3M Company - Health Care Business 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack recall — FDA Z-2640-2023
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam…
Class IIFDA: Ongoing3M Company - Health Care Business
Medical DeviceOct 4, 2023
Covidien Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm recall — FDA Z-2632-2023
Some catheter kits labeled as 23 cm implant length incorrectly included catheters of 28 cm implant length; the actual catheter implant length is identifiable based upon the correct labeling…
Class IIFDA: OngoingCovidien LP
Medical DeviceOct 4, 2023
B. Braun Medical B. Braun NORM-JECT Luer Solo, 10 ml, Sterile-Intended to be used to deliver recall — FDA Z-2643-2023
The sterile blister packaging may be damaged, and sterility may be compromised
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceOct 4, 2023
Inmar Supply Chain Solutions Various Medical Products stored on pallets, including but not recall — FDA Z-2634-2023
Various medical devices potentially exposed to rodent and rodent activity. In addition, medical devices may have been subjected to temperatures in excess of storage requirements on product…
Class IIFDA: OngoingInmar Supply Chain Solutions, LLC
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Recent recall archives
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September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories