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Family Dollar Stores, Llc.

Family Dollar Stores, Llc. Recalls

All product recalls associated with Family Dollar Stores, Llc..

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Recall Summary

Total Recalls

1000

Past Year

100

Class I (Serious)

Most Recent

Dec 2025

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 601–620 of 2670 recalls

Aveeno Daily Moisturizing Lotion (Family Dollar) – temperature storage issue (2022)

cGMP deviations: product stored outside of labeled temperature requirements.

Class IIModerate

FDAMay 17, 2022Nationwide• Family Dollar Stores, Llc.

Wolverine RMAX Vehicles (Yamaha) - fire explosion risk (2022)

Fire/Burn Risk

This recall involves Off-Road Side-by-Side vehicles with model numbers YXF10WPZMG (Wolverine RMAX 4 SE), YXF10WPLML (Wolverine RMAX 4 LE), YXF10WPAMS (Wolverine RMAX 4), YXE10WPZMG (Wolverine RMAX 2 SE), YXE10WPAMS/YXE10WPAMW (Wolverine RMAX 2), and YXE10WPLML (Wolverine RMAX 2 LE). The side-by-side vehicles were sold in silver, white, black, yellow, gray and blue colors. The model name Wolverine RMAX is printed on the right and left sides of the vehicles. The model number is located on top of the airbox. The Vehicle Identification Number (VIN) can be found on the vehicle frame behind the left rear wheel. VIN numbers included in this recall are ***AN44Y***101342 ***AN39Y***102877. The VIN range is sequential in the last six digits 101342-102877.

CPSCMay 12, 2022Nationwide• Yamaha Motor Manufacturing Corp of America, of Newnan, Georgia

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Alcon Clareon IOL (Alcon) – Mislabeling Risk (2022)

Due to device (preloaded intraocular lens) mislabeling, associated with partial mixing of product during overlapping manufacturing runs, and attributed to improper manufacturing line clearance.

FDAMay 11, 2022AL, CA, FL +13 more• Alcon Laboratories Ireland, Ltd Cork Business And Technology Park Model Farm Road Cork Ireland

Thor Sanctuary (Thor) – LPG Fitting Issue (2022)

Fire/Burn Risk

Thor Motor Coach (TMC) is recalling certain 2022 Scope, Tellaro, Sanctuary, Delano, Sequence, Tranquility, Rize, Synergy, Quantum, Magnitude, Geneva, Compass, Chateau, Four Winds, and 2022-2023 Tiburon, and Gemini vehicles. The quick disconnect fittings in the LP gas system may be cracked, causing a gas leak.

NHTSAMay 5, 2022Nationwide• THOR MOTOR COACH

Ratcheting Screwdriver Handle (Tornier) – Sterilization Concern (2022)

The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container.

FDAMay 3, 2022Nationwide• Tornier, Inc

STORZ KARL STORZ-ENDOSKOPE (Karl Storz) – image loss risk (2022)

The endoscope may experience a loss of image when activating monopolar electrocautery, due a manufacturing assembly process issue.

FDAMay 3, 2022Nationwide• Karl Storz Endoscopy

Hand Sanitizer (Torco Race Fuels) – Chemical Contamination (2022)

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Class IIModerate

FDAApr 21, 2022IN• Torco Race Fuels

Lansoprazole Orally Disintegrating Tablets (Dr. Reddy's) – Dissolution Failure (2022)

Failed Dissolution Specifications

Class IIModerate

FDAApr 15, 2022OH• Dr. Reddy's Laboratories, Inc.

BioPlex 2200 ToRC IgM (Bio-Rad) – Performance Concerns (2022)

Performance concerns for the CMV IgM analyte. Analyte has demonstrated variable elevated background depending on the handling of the reagent pack.

FDAApr 14, 2022Nationwide• Bio-Rad Laboratories, Inc.

Pantoprazole Sodium Tablets (Torrent) – Tablet Cracking (2022)

CGMP deviations: tablets cracking

Class IIModerate

FDAApr 11, 2022Nationwide• Torrent Pharma Inc

HemosIL ReadiPlasTin (Instrumentation Lab) – QC Result Variability (2022)

Variable and out of specification QC results with HemosIL ReadiPlasTin. IL will remove all lots from the market and convert customers to an alternative prothrombin time (PT) reagent, specifically HemosIL RecombiPlasTin 2G.

FDAApr 8, 2022Nationwide• Instrumentation Laboratory

Variant Sickle Cell CD-ROM (Bio-Rad) – Software Issue (2022)

The problem is with the Bio-Rad VARIANT nbs Sickle Cell Program Resin Update CD-ROM software; Model Number: 250-3020, included in VARIANT nbs Sickle Cell Progam Reorder Pack #250-3000. This CD-ROM software included in specific lots of VARIANT nbs Sickle Cell Progam Reorder Pack causes all customized settings in the Setup/Test/Data Setup subscreen and Setup/Test/Pattern Setting subscreen to be overwritten with the default settings when the Update Kit procedure is performed.The VARIANTnbs Sickle Cell Program has been validated using the default Resin Update CDROM parameters for the intended use. However, there is a risk that the customer's custom pattern settings may be different than the default settings, resulting in a different pattern being assigned to some samples that the laboratory has validated. Following the complaints from 4 customers who experienced these issues, the firm initiated this recall.

FDAApr 7, 2022AL, AZ, AR +21 more• Bio-Rad Laboratories, Inc.