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Beaumont Bio-med, Inc.

Beaumont Bio-med, Inc. Recalls

All product recalls associated with Beaumont Bio-med, Inc..

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Recall Summary

Total Recalls

1000

Past Year

566

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 4201–4220 of 7756 recalls

Muscle & Joint Pain Relief Formula (Beaumont Bio-med) – Microbial Risk (2018)

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Class IIModerate

FDAAug 31, 2018Nationwide• Beaumont Bio-med, Inc.

Sore Throat Response Formula (Beaumont Bio-med) – Microbial Risk (2018)

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Class IIModerate

FDAAug 31, 2018Nationwide• Beaumont Bio-med, Inc.

Arthritis Pain Relief Formula (Beaumont Bio-med) – Microbial Risk (2018)

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

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Class IIModerate

FDAAug 31, 2018Nationwide• Beaumont Bio-med, Inc.

Diarrhea Response Formula (Beaumont Bio-med) – contamination risk (2018)

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Class IIModerate

FDAAug 31, 2018Nationwide• Beaumont Bio-med, Inc.

NeoRelief Muscle Gel (BioLyte) – ingredient contamination (2018)

CGMP Deviations: finished product produced with active ingredients recalled by the manufacturer, King Bio Inc., due to water contamination issues that could potentially affect the quality of this product.

Class IIModerate

FDAAug 31, 2018Nationwide• BioLyte Laboratories, LLC

Cybex Smith Press (Cybex International) – Serious Injury Risk (2018)

This recall involves the Cybex Smith Press model 5340, manufactured and distributed from 1989 through 1993, and model 5341, manufactured and distributed from 1993 through 2009. The models have a weight bar seated between two parallel vertical tracks on latch pins. The weight bar can be moved up and down to perform upper body and lower body exercises. The equipment is used primarily in fitness facilities. The weight bar was sold with the Smith Press, and the weights were sold separately. The model number is printed on the base of the frame of the Smith Press equipment.

CPSCAug 29, 2018Nationwide• Cybex International Inc., of Owatonna, Minn.

MethylPREDNISolone Tablets (Jubilant Cadista) – Stability Failure (2018)

Failed Stability Specifications: An out-of-specification result was obtained during 18-month stability testing for assay.

Class IIILow

FDAAug 27, 2018Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Landmaster Utility Vehicles (American Landmaster) – Fire Hazard (2018)

Fire/Burn Risk

This recall involves model year 2018 gasoline-powered Landstar, Crossroad and Trailwagon models of American Landmaster four-wheel off-road utility vehicles. The recalled vehicles were sold in a variety of colors. The model name and number are printed on the hood of each front fender. The American Landmaster logo is printed on the center of the hood of the vehicle. The VIN is located behind the pedals and below the steering wheel. Model Number VIN range start VIN range end CR350, LS350, LS350DL A4PUTYFB1JBA00023 A4PUTYFB9JBA00304 A4PUTYFB1JBA00751 A4PUTYFB7JBA00754 LS450 A4PUTYJC4JBA00422 A4PUTYJC6JBA00499 A4PUTYJC3JBA00749 A4PUTYJCXJBA01512 TW450 A4PUTYJCXJBA00358 A4PUTYJC0JBA00496 A4PUTYJC2JBA00760 A4PUTYJC2JBA01147 TW750 A4PUTYPD0JBA00014 A4PUTYPD8JBB00149 LS477 A4PUVTKD7JBB00003 A4PUVTKD9JBB00049 LS550 A4PUTVKD9JBA00003 A4PUTVKD9JBA00308 LS670, 677EFI, 677EPS A4PUTYPD6JBB00005 A4PUTYPD7JBB00224 Crew2, Crew4, Crew4X A4PUFYPD0JBA00005 A4PUFYPD5JBA00078

CPSCAug 23, 2018Nationwide• ASW, LLC d/b/a American Landmaster, of Columbia City, Ind.

Sodium Chloride Injection (Baxter Healthcare) – CGMP Deviation (2018)

CGMP Deviations

Class IIModerate

FDAAug 21, 2018MS, TX• Baxter Healthcare Corporation

Premo Turkey Sandwich (Lipari Foods) – Listeria Risk (2018)

Listeria

Potential contamination of Listeria monocytogenes

Class IIModerate

FDAAug 21, 2018IL, IN, KY +9 more• Lipari Foods Operating Company, LLC dba JLM Manufacturing

Natural Cocoa Butter (Blommer) – Process deviation (2018)

CCP process deviation, Critical limit not met

Class IIModerate

FDAAug 17, 2018IL, NJ• Blommer Chocolate Co., Inc.

Valsartan Tablets (Jubilant Cadista) – Incorrect Excipient (2018)

Undeclared Allergen

Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.

Class IIILow

FDAAug 14, 2018Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Diltiazem HCl Capsules (Mylan) – Impurity Specifications (2018)

Failed Impurities/Degradation Specifications; out of specification results for related compound per the manufacturer

Class IIILow

FDAAug 14, 2018Nationwide• Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Valsartan Tablets (Jubilant Cadista) – Incorrect Excipient (2018)

Undeclared Allergen

Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.

Class IIILow

FDAAug 14, 2018Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Valsartan Tablets 40mg (Jubilant Cadista) – incorrect excipient (2018)

Undeclared Allergen

Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.

Class IIILow

FDAAug 14, 2018Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Valsartan Tablets (Jubilant Cadista) – Incorrect Excipient (2018)

Undeclared Allergen

Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.

Class IIILow

FDAAug 14, 2018Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Alprostadil Injectable (Westlab) – Incorrect Formulation (2018)

Incorrect Product Formulation

Class IIModerate

FDAAug 10, 2018Nationwide• Westlab Pharmacy, Inc. dba Westlab Pharmacy

Cyclosporine Eye Drops (Westlab) – Process Control Issue (2018)

Lack of Process Controls

Class IIModerate

FDAAug 10, 2018Nationwide• Westlab Pharmacy, Inc. dba Westlab Pharmacy

Cataract Drops (Westlab) – Process Control Issue (2018)

Lack of Process Controls

Class IIModerate

FDAAug 10, 2018Nationwide• Westlab Pharmacy, Inc. dba Westlab Pharmacy

Steak Marinade (King's Food Products) – Undisclosed Ingredients (2018)

Undeclared Allergen

Deli Star Inc. dba King's Food Products initiated a voluntary recall of Chef s Request professional steak marinade and Buckhead wildlife marinade due to undeclared allergens soy and wheat.

Class IIModerate

FDAAug 9, 2018IL, VA• Deli Star Ventures Inc. dba King's Food Products