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Blount Fine Foods Corporation

Blount Fine Foods Corporation Recalls

All product recalls associated with Blount Fine Foods Corporation.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1961–1980 of 7756 recalls

Southwest Corn Chowder (Panera) – Contains Undeclared Wheat (2022)

Undeclared Gluten

Contains undeclared wheat

Class IHigh

FDAJun 22, 2022CA, IL, IA +9 more• Blount Fine Foods Corporation

Blue Kuna Taste of Devil's Night Heat BBQ Sauce (FEAST Detroit) – mislabeled vegan (2022)

The product was mislabeled as Vegan Product but contains anchovies

Class IIModerate

FDAJun 21, 2022MI• Food Entrepreneur Accelerator and Startup Terminal, DBA FEAST Detroit

Bard Access Systems, Inc.: Intraosseous needle and driver. Catalog/Device Name: ...

BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss of intraosseous access; 2) Stylet safety mechanism may not engage as the stylet is removed; 3) Metal discs in the powered driver may stick rendering the driver unusable.

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FDAJun 20, 2022Nationwide• Bard Access Systems, Inc.

Morphine Sulfate 60mg Tablets (Bryant Ranch) – Labeling Mix-up (2022)

Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.

Class IHigh

FDAJun 17, 2022AL, IN• Bryant Ranch Prepack, Inc.

Morphine Sulfate 30mg Tablets (Bryant Ranch) – Labeling Mix-up (2022)

Class IHigh

FDAJun 17, 2022AL, IN• Bryant Ranch Prepack, Inc.

Kroger Arthritis Pain Acetaminophen (Aurobindo Pharma) – packaging issue (2022)

This recall involves the Kroger brand acetaminophen. The red, white, and yellow label states, Kroger, Acetaminophen, Arthritis Pain, Extended-Release, Tablets USP, 650 mg, 225 extended-release tablets. The bottle has a red continuous thread gear closure. UPC number 041260012846 and lot numbers P2100890, P2100891, P2100992 (each with expiration date Aug-2023) and P2101010 (with expiration date Apr-2023) are included in this recall. The UPC number, lot number and expiration date are printed near the drug facts panel on the label on the back of the bottle.

CPSCJun 16, 2022Nationwide• Aurobindo Pharma Limited, of Telangana, India

Walgreens Pain Reliever Acetaminophen (Aurobindo Pharma) – packaging issue (2022)

This recall involves the Walgreens brand acetaminophen product. The red and white label states Walgreens, Easy Open for Adults, Pain Reliever, Acetaminophen, 500 mg, Fever Reducer, Extra Strength, 150 caplets. The bottle has a red continuous thread gear closure. UPC number 311917218090 and Lot numbers P2100627, P2100671, P2100672, P2100689 P2100747, P2100859 (each with expiration date Nov-2022) and P2200050 (with expiration date Jan-2023) are included in this recall. The UPC number, lot numbers and expiration date are printed near the drug facts panel on the label on the back of the bottle.

CPSCJun 16, 2022Nationwide• Aurobindo Pharma Limited, of Telangana, India

Draximage MAA Kit (Jubilant) – Sterility Concern (2022)

Lack of Assurance of Sterility: Out-of-specification test results obtained for Endotoxin testing.

Class IIModerate

FDAJun 16, 2022Nationwide• Jubilant Draximage Inc

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation 11B

This notice concerns two issues found related to the display of Linear Energy Transfer (LET) in RayStation 11B including some service packs. First, when using a dose threshold for an evaluation dose, LET display might be misleading. Second, a displayed beam-specific LET distribution can sometimes be out of sync with the selected beam.

FDAJun 10, 2022Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland: Soluble Transferrin Receptors (STFR), Catalog Number TF10...

A customer reported a problem with the reagent and calibrator. Randox Laboratories carried out an investigation and confirmed the issue. The complaint is pertaining to atypical calibration curves that can results in non-numerical results. This affects Siemens Atellica CH analysers only. Customer have reported an atypical calibration curve that results in the values around the low QC range to produce a non-numerical result. It appears to be related to the bottle values of the calibrator producing a curve shape that is too linear for the logitlog calculation to calculate. This issue can only be identified in the Atellica graphical view of the calibration. In most of the cases when this has occurred, it is picked up by the QC generating a Math Error, however, there are reports of QC shifts after calibration without the Math Error flagged that may be related to this issue. Results reported with STFR Level 1, with a concentration less than 1.7mg/L, using TF10159 and TF10161 can be underestimated by up to 30%. This issue has been reported with reagent lots 575475 and 562691, calibrator lots 537725 and 562696. No other complaints received.

FDAJun 9, 2022Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Abbott Laboratories: REF: 08P4377, Alinity c Hemoglobin Reagent Kit, IVD, CE...

There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.

FDAJun 9, 2022AL, AK, AZ +40 more• Abbott Laboratories

Abbott Laboratories: REF: 08P4320, Alinity c Hemoglobin Reagent Kit, IVD, CE...

There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.

FDAJun 9, 2022AL, AK, AZ +40 more• Abbott Laboratories

Abbott Laboratories: REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, ...

There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.

FDAJun 9, 2022AL, AK, AZ +40 more• Abbott Laboratories

Intimidator and Mahindra UTVs – Crash Hazard (2022)

This recall involves Intimidator and Mahindra branded models 750, 800, 1000, TGB, and GC1K utility vehicles (UTVs). The recalled UTVs were sold in a variety of colors. "Intimidator" or "Mahindra" is displayed on the front grill and the model series is printed on the rear-side panels. The vehicle identification number (VIN) can be found on a label inside the glove box, inside the hood compartment and below the driver's seat. The serial numbers of affected Intimidator vehicles are available at www.intimidatorutv.com/recall/. The serial range of the affected Mahindra vehicles are 000000 through 010545. The following vehicles are included in this recall: Make & Model Model Years Intimidator GC1K Classic 2018-2022 Intimidator GC1K Crew 2019-2022 Intimidator GC1K Truck 2019-2022 Intimidator 750 Classic 2013-2022 Intimidator 750 Crew 2014-2022 Intimidator 750 Truck 2013-2022 Intimidator 800 Classic 2015-2018 Intimidator 800 Crew 2015-2018 Intimidator 800 Enforcer 2016-2018 Intimidator 1000 Series Diesel Classic 2013-2022 Intimidator 1000 Series Diesel Crew 2013-2022 Intimidator 1000 Series Diesel Truck 2013-2022 Mahindra 750 Classic 2015-2020 Mahindra 750 Crew 2015-2020 Mahindra 750 Truck 2015-2020 Mahindra TGB Classic 2015-2020 Mahindra TGB Crew 2015-2020 Mahindra 1000 Diesel Classic 2015-2020 Mahindra 1000 Diesel Crew 2015-2020 Mahindra 1000 Diesel Truck 2015-2020

CPSCJun 9, 2022Nationwide• Intimidator, of Batesville, Ark.

Milk Chocolate Covered Blueberries (Wilbur's) – Undeclared Almonds (2022)

Undeclared Allergen

Product contains undeclared almonds.

Class IHigh

FDAJun 8, 2022Nationwide• Wilbur's Of Maine Chocolate Confections

Pedialyte Immune Support (Abbott) – Container Leakage (2022)

These products are being recalled due to the potential of leakage from the 1L container.

Class IIModerate

FDAJun 3, 2022AL, AZ, AR +25 more• Abbott Laboratories

Pedialyte Immune Support (Abbott) – Container Leakage (2022)

These products are being recalled due to the potential of leakage from the 1L container.

Class IIModerate

FDAJun 3, 2022AL, AZ, AR +25 more• Abbott Laboratories

Pedialyte (Abbott) – Undeclared Wheat (2022)

The third party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder, which is not declared on the label.

Class IIILow

FDAJun 3, 2022AZ, CA, FL +9 more• Abbott Laboratories

CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. No. 235 Longhutangjieban Chuangxindadao Xinbei Changzhou China: DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anato...

One lot of DVRASL plates were incorrectly etched and may have been placed into kits as DVRAR or DVRASR plates

FDAJun 2, 2022Nationwide• CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. No. 235 Longhutangjieban Chuangxindadao Xinbei Changzhou China

Backcountry Access Tracker4 Transceivers (Backcountry Access) – Loss Risk (2022)

This recall involves the Backcountry Access Tracker4 Avalanche Transceiver sold in yellow and black. The transceiver has a digital screen on the front and is about five inches long and three inches wide. "BCA" and the model name "Tracker4" are printed on the front of the unit. The serial number for a transceiver is located inside the battery compartment after removing the top AAA battery. Only the transceivers with serial numbers beginning with 21H05 or 21H06 are affected by this recall.

CPSCJun 2, 2022Nationwide• Backcountry Access, Inc.