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Cubist Pharmaceuticals, Inc.

Cubist Pharmaceuticals, Inc. Recalls

All product recalls associated with Cubist Pharmaceuticals, Inc..

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

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 13281–13300 of 17593 recalls

Cubicin Injection (Cubist) – Glass Particulates (2013)

Presence of Particulate Matter; Glass particulates observed in vials

Class IHigh

FDAAug 29, 2013Nationwide• Cubist Pharmaceuticals, Inc.

NyQuil Cold & Flu (Procter & Gamble) – Packaging Mix-up (2013)

Undeclared Allergen

Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were inadvertently overwrapped with NyQuil Liquid Cherry information as a result the outer wrap does not correctly identify color additives, particularly FD&C Yellow No. 6 and FD&C Yellow 10.

Class IIModerate

FDAAug 29, 2013Nationwide• Procter & Gamble Co

2013 CAN-AM SPYDER ST Recall: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER

1...663 664665666 667...880

Page 665 of 880Next

Fire/Burn Risk

Bombardier Recreational Products (BRP) is recalling certain model year 2013 Can-Am Spyder RT series and ST series motorcycles. The tandem brake master cylinder manifold inlet may melt allowing the brake fluid to leak out.

NHTSAAug 28, 2013Nationwide• CAN-AM

Chocolate Raisins (American Importing) – mislabeled package (2013)

It was discovered that a package of Milk Chocolate Peanuts was erroneously labeled as Milk Chocolate Raisins.

Class IIModerate

FDAAug 26, 2013CA, CO, IN +6 more• American Importing Co, Inc

Glutathione Injectable (Creative Compounds) – Contamination Risk (2013)

Glutathione 100 mg/mL injectable human drug is recalled due to Out Of Specification results or potential bacterial contamination and it was reported as passing by a contract laboratory.

Class IIModerate

FDAAug 23, 2013OR, WA• Creative Compounds

Multitrace-5 Concentrate (South Coast) – Sterility Concern (2013)

Lack of Assurance of Sterility: Park Compounding is recalling Methylcobalamin 5 mg/mL, Multitrace-5 Concentrate, and Testosterone Cypionate (sesame oil) for injection due to lack of sterility assurance.

Class IIModerate

FDAAug 23, 2013CA, IN• South Coast Specialty Compounding, Inc.

Methylcobalamin Injection (South Coast) – Sterility Concern (2013)

Class IIModerate

FDAAug 23, 2013CA, IN• South Coast Specialty Compounding, Inc.

Testosterone Cypionate (South Coast) – Sterility Concern (2013)

Lack of Assurance of Sterility: Park Compounding is voluntarily recalling two lots of Methylcobalamin 5mg/ml and Multitrace-5 Concentrate, and one lot of Testosterone Cypionate (sesame oil) for injection due lack of sterility assurance.

Class IIModerate

FDAAug 23, 2013CA, IN• South Coast Specialty Compounding, Inc.

Hartley's Salt & Vinegar Chips (Hartleys) – Undeclared Milk (2013)

Undeclared Allergen

Undeclared lactose (milk) in seasoning sub-ingredient used in the manufacturing of Hartley's Salt & Vinegar Potato Chips.

Class IHigh

FDAAug 20, 2013PA• Hartleys Potato Chip Company Inc

LipiChol 540 (XYMOGEN) – Incorrect Labeling (2013)

Product was labeled as a medical food as opposed to a dietary supplement.

Class IIILow

FDAAug 16, 2013Nationwide• Atlantic Pro Nutrients, Inc. dba XYMOGEN

LipiChol Omega-3 (XYMOGEN) – Incorrect Labeling (2013)

Product was labeled as a medical food as opposed to a dietary supplement.

Class IIILow

FDAAug 16, 2013Nationwide• Atlantic Pro Nutrients, Inc. dba XYMOGEN

Endura Ambient LED Bulbs (Philips) – Shock Hazard (2013)

This recall involves Endura 12-watt and Ambient 12.5-watt LED dimmable light bulbs. The bulbs are orange in color and have "MADE IN CHINA," "Fabrique in Chine" followed by a slanted "S," and the model number 9290001829 printed on the gray plastic band on the neck of the bulbs. The date codes, 2L for the Endura bulbs and 2K or 2L for the Ambient bulbs, are printed on the metal screw base. The bulbs give off a white light and are used indoors to replace incandescent bulbs. The following chart outlines the recall details: Product Name Model Number Ordering Code UPC Date Code EnduraLED 12W A19 2700k Dimmable 120V 9290001829 12A19/END/2700-800 DIM 46677 40994 2L AmbientLED 12.5W A19 2700k Dimmable 120V 9290001829 BC-12.5A19/AMB/2700-800 DIM 46677 42215 2K and 2L

CPSCAug 15, 2013Nationwide• Philips Lighting Co., of Somerset, N.J.

72HP Male Enhancement (Fabscout) – Undeclared Sildenafil (2013)

Undeclared Allergen

Marketed without an Approved NDA/ANDA: products were found to contain undeclared sildenafil

Class IHigh

FDAAug 14, 2013CA, FL, UT• Fabscout Entertainment, Inc

Evil Root Supplement (Fabscout) – Undeclared Sildenafil (2013)

Undeclared Allergen

Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil

Class IHigh

FDAAug 14, 2013CA, FL, UT• Fabscout Entertainment, Inc

Lidocaine Hydrochloride Injection (Novocol) – Subpotent Drug (2013)

Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000 Injectable, distributed under the names: Octocaine 100, and 2% Xylocaine Dental, may be subpotent for the epinephrine component.

Class IIModerate

FDAAug 14, 2013Nationwide• Novocol Pharmaceutical of Canada

Pro Power Max Energy Enhancer (Fabscout) – Undeclared Drugs (2013)

Undeclared Allergen

Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil and tadalafil

Class IHigh

FDAAug 14, 2013CA, FL, UT• Fabscout Entertainment, Inc

Compact Utility Tractors (John Deere) – Serious Injury Risk (2013)

This recall involves 19 models of John Deere 1000, 2000, 3000 and 4000 series compact utility tractors manufactured between February 2013 and July 2013. The tractors are green and yellow with a foldable black, metal rollover protection bar that extends above the operator's head. The model number is on the hood. The serial number is located on the right hand side of the frame above the front axle. Compact utility tractors with serial numbers in the following ranges are included in this recall: Model Number Vehicle Identification Number Ranges 1023E 1LV1023EXXX310006 to 1LV1023EXXX310083 1025R 1LV1025RXXX111788 to 1LV1025RXXX116214 2025R 1LV2025RXXX110121 to 1LV2025RXXX110202 2032R 1LV2032RXXX110008 to 1LV2032RXXX110283 2320H 1LV2320HXXX712151 to 1LV2320HXXX712593 2520H 1LV2520HXXX811702 to 1LV2520HXXX811703 2720H 1LV2720HLCH511543 (Only) 3320H 1LV3320HXXX910198 to 1LV3320HXXX910700 3320P 1LV3320PXXX910129 to 1LV3320PXXX910299 3520H 1LV3520HXXX910239 to 1LV3520HXXX910579 3520P 1LV3520PXXX910098 to 1LV3520PXXX910188 3720H 1LV3720HXXX910181 to 1LV3720HXXX910429 4120H 1LV4120HXXX916152 to 1LV4120HXXX916350 4120P 1LV4120PXXX916013 to 1LV4120PXXX916014 4320H 1LV4320HXXX916166 to 1LV4320HXXX916420 4320P 1LV4320PXXX916036 to 1LV4320PXXX916112 4520H 1LV4520HXXX916127 to 1LV4520HXXX916276 4520P 1LV4520PXXX916034 to 1LV4520PXXX916135 4720H 1LV4720HXXX916129 to 1LV4720HXXX916919

CPSCAug 14, 2013Nationwide• Deere & Company, of Moline, Ill.

Specialty Compounding Products (Specialty Compounding) – Sterility Concerns (2013)

Lack of Assurance of Sterility

Class IIModerate

FDAAug 9, 2013Nationwide• Specialty Compounding, LLC

Calcium Gluconate Injection (Specialty Compounding) – Microbial Contamination (2013)

Non Sterility: Microbial contamination

Class IHigh

FDAAug 9, 2013Nationwide• Specialty Compounding, LLC

Playmat Set (Holgate) – Choking Risk (2013)

Choking Hazard

The Wegmans Playmat Set includes a 24-inch by 30-inch cotton canvas playmat and four toy wooden vehicles. The toy vehicles include a blue car, a red "Wegmans" delivery van, a green "Wegmans" farm tractor and a yellow "School Bus." The sets were sold in a yellow box measuring about 12-inches by 12-inches with "Wegmans Playmat Set," an age label circle with "2+" and "Made in the USA" printed on the front of the box. UPC Code 0 7789028735 4 is printed on the back of the box.

CPSCAug 8, 2013Nationwide• Holgate Toy Division, of Pepperell Braiding Co Inc., of Pepperell, Mass.