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American Family Pharmacy, LLC

American Family Pharmacy, LLC Recalls

All product recalls associated with American Family Pharmacy, LLC.

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Recall Summary

Total Recalls

1000

Past Year

579

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 7641–7660 of 10937 recalls

Assured Aspirin (American Family) – Subpotent Tablets (2014)

Subpotent Drug: Product failed to meet USP Specifications on assay, content uniformity, and dissolution.

Class IIModerate

FDASep 15, 2014CA, VA, WA• American Family Pharmacy, LLC

Whole Roma Tomatoes (Taylor Farms) – Salmonella Potential (2014)

Salmonella

Firm was notified by supplier that specific lots of "expo fresh" Roma tomatoes may be contaminated with Salmonella.

Class IHigh

FDASep 12, 2014AZ, CA, NV +1 more• Taylor Farms Pacific Inc. (MacArthur Facility)

Sicilian Vegetable Salad (Taylor Farms) – Salmonella Risk (2014)

Salmonella

Firm was notified by supplier that specific lots of "expo fresh" Roma tomatoes may be contaminated with Salmonella.

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Class IHigh

FDASep 12, 2014AZ, CA, NV +1 more• Taylor Farms Pacific Inc. (MacArthur Facility)

Diced Roma Tomatoes (Boskovich Farms) – Salmonella Risk (2014)

Salmonella

Boskovich Farms is recalling Roma Tomatoes because they may be contaminated with Salmonella.

Class IHigh

FDASep 12, 2014CA• Boskovich Farms, Inc

Roma Tomatoes (Boskovich Farms) – Salmonella Contamination (2014)

Salmonella

Boskovich Farms is recalling Roma Tomatoes because they may be contaminated with Salmonella.

Class IHigh

FDASep 12, 2014CA• Boskovich Farms, Inc

Wildcat Trail Side by Side (Arctic Cat) – Fire Hazard (2014)

Fire/Burn Risk

This recall involves all 2014 Arctic Cat Wildcat Trail and Wildcat Trail XT side-by-side utility vehicles with Vehicle Identification Numbers (VIN) 000001 through 316232. The VIN is located on the frame tube near the driver's side front wheel. These units were sold in red, green, lime green, team arctic green and mat black. The words "Arctic Cat" and "Wildcat Trail" appear on the sides of these vehicles and on the hood.

CPSCSep 11, 2014Nationwide• Arctic Cat, Inc., of Thief River Falls, Minn.

Philips Medical Systems (Cleveland) Inc: The Ingenuity CT, Ingenuity Core, and Ingenuity Core128 s...

Ingenuity CT system can mislabel the exposure that results in an image in the incorrect order that it was taken by the user.

Class IIModerate

FDASep 11, 2014AZ, CA, CT +8 more• Philips Medical Systems (Cleveland) Inc

Humidifiers (Great Innovations) – Fire Hazard (2014)

Fire/Burn Risk

This recall involves Air Innovations branded Ultrasonic Clean Mist humidifiers with mood lights. Model number MH-407 and date code MX1342, MX1343, MX1344, MX1344, MX1345 or MX1346 are printed on a label affixed to the underside of the humidifier. The recalled humidifiers are 15 inches high and were sold in four colors: black, silver, red and blue. A mood light button and the words "Air Innovations" are on the front of the one-gallon humidifiers. QVC item number V32459 is printed on the packing slip shipped with the humidifier.

CPSCSep 3, 2014Nationwide• Great Innovations LLC, of Miramar, Fla

Chinese Style Noodles (Phoenix Produce) – undeclared coloring (2014)

Undeclared Allergen

Phoenix Produce is recalling Chinese Style Noodles because it contains undeclared FD&C Yellow No. 5, Yellow No. 6, and Red No. 40.

Class IIModerate

FDAAug 29, 2014AZ• Phoenix Produce & Noodle Company, LLC.

Liquid Vitamin C (Hi-Tech Pharmacal) - Low Active Ingredient (2014)

The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active ingredient is at a lower level than stated on the label.

Class IIILow

FDAAug 25, 2014CA, FL, ID +10 more• Hi-Tech Pharmacal Co., Inc.

Maquet Medical Systems USA: TEGRIS System manufactured by MAQUET GMBH in Germany The...

The wrong movement results on the MAGNUS OR table. The button commands on the TEGRIS touchscreen for Lower Leg Up and Upper Leg Down are switched in the software for the integration with the MAGNUS operating table system.

Class IIModerate

FDAAug 21, 2014Nationwide• Maquet Medical Systems USA

Philips Medical Systems, Inc.: Ingenia, Intera, Achieva and Achieve dStream MR systems o...

When a fused series of a sagittal, coronal or radial multi station scan is generated in MobiView, the resultant image order is reversed. This occurs with software release R5.1.7/R5.1.8.

Class IIModerate

FDAAug 21, 2014Nationwide• Philips Medical Systems, Inc.

Terumo Cardiovascular Systems Corporation: Hercules 360 Universal Stabilizing Arm, top mount, 360-de...

Terumo Cardiovascular Systems (Terumo CVS) is recalling certain lots of Hercules TM 360 Universal Stabilizing Arms because the two pins that hold the sleeve attached to the distal end of the device may come loose, causing the pins and sleeve to separate from the device. While the arm can still function without the pins and sleeve in place, there is potential for the loose components to fall into the surgical site.

Class IIModerate

FDAAug 20, 2014Nationwide• Terumo Cardiovascular Systems Corporation

Mason Convertible Cribs (Bexco) - Fall Hazard (2014)

This recall includes Franklin & Ben Mason style 4-in-1 style cribs model number 5601 that were manufactured from January 2012 through August 2012. The model number and the date of manufacture are printed on a label on the inside of a side panel of the crib. Listed on the label as a "serial number," the following purchase order numbers are included in the recall: H004522, H004546, H004548 or H004777. The cribs have solid wood sideboards and wood rails on the front and back of the crib in varying heights and can convert to a daybed, toddler bed or full-sized bed. There is a storage drawer at the base of the crib with two metal knobs. The recalled cribs were sold in weathered gray and rustic brown, and measure 57 inches long by 33 inches wide by 51 inches high.

CPSCAug 19, 2014Nationwide• Bexco Enterprises Inc., of Montebello, Calif.

ICU Medical, Inc.: 83" (211 cm) Appx 10.3 mL, 60 Drop Primary Set w/BCV-Clav...

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

St Jude Medical Cardiac Rhythm Management Division: Ellipse Implantable Cardioverter Defibrillators (ICDs), ...

An anomaly may result in delayed, partial, or no delivery of high voltage therapy. Internal damage to the high voltage capacitors, which may result in extended charge time, occurring during capacitor maintenance or charging for high voltage therapy. It may present as a vibratory patient notification and upon interrogation, a programmer or Merlin.net alert.

Class IIModerate

FDAAug 19, 2014Nationwide• St Jude Medical Cardiac Rhythm Management Division

ICU Medical, Inc.: STAT 2 Flow Controller; 80" (203 cm) Appx 14.8 mL, 60 Dro...

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

ICU Medical, Inc.: 98" (249 cm) Appx 12.3 ml, 60 Drop Primary Set w/Pre-Slit...

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.

Philips Medical Systems, Inc.: Patient Support Material Number: 9890 010 87431, used wit...

The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.

Class IIModerate

FDAAug 19, 2014AZ, CT, FL +9 more• Philips Medical Systems, Inc.

ICU Medical, Inc.: STAT 2 Flow Controller; 80" (203 cm) Appx 14.8 mL, 20 Dro...

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

Class IHigh

FDAAug 19, 2014Nationwide• ICU Medical, Inc.