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Gorant Candies Inc A Division of Carlton Cards Retail Inc

Gorant Candies Inc A Division of Carlton Cards Retail Inc Recalls

All product recalls associated with Gorant Candies Inc A Division of Carlton Cards Retail Inc.

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Recall Summary

Total Recalls

398

Past Year

Class I (Serious)

Most Recent

Oct 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 301–320 of 398 recalls

No Sugar Added Chocolate Peanuts (Gorant Candies) – Contamination Risk (2009)

Salmonella

The product is being recalled because it was manufactured using peanuts that were recalled by Peanut Corporation of America because of their potential to be contaminated with Salmonella.

Class IHigh

FDAFeb 3, 2009AL, AZ, AR +26 more• Gorant Candies Inc A Division of Carlton Cards Retail Inc

Milk Chocolate Peanuts (Gorant Candies) – Contamination Risk (2009)

Salmonella

The product is being recalled because it was manufactured using peanuts that were recalled by Peanut Corporation of America because of their potential to be contaminated with Salmonella.

Class IHigh

FDAFeb 3, 2009AL, AZ, AR +26 more• Gorant Candies Inc A Division of Carlton Cards Retail Inc

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Chocolate Bridge Mix (Gorant Candies) – Contamination Risk (2009)

Salmonella

The product is being recalled because it was manufactured using peanuts that were recalled by Peanut Corporation of America because of their potential to be contaminated with Salmonella.

Class IHigh

FDAFeb 3, 2009AL, AZ, AR +26 more• Gorant Candies Inc A Division of Carlton Cards Retail Inc

No Sugar Added Bridge Mix (Gorant Candies) – Contamination Risk (2009)

Salmonella

The product is being recalled because it was manufactured using peanuts that were recalled by Peanut Corporation of America because of their potential to be contaminated with Salmonella.

Class IHigh

FDAFeb 3, 2009AL, AZ, AR +26 more• Gorant Candies Inc A Division of Carlton Cards Retail Inc

Rheem Oil-Fired Furnaces (Rheem) – Fire Hazard (2009)

Fire/Burn Risk

This recall involves oil-fired furnaces sold under the Rheem, Ruud and United Refrigeration brands. Only the models beginning with the model numbers listed in the chart below and with date codes ending in 0106 through 5206, 0107 through 5207, or 0108 through 4808 are included in this recall. The model number and date code (designated by the four digits following an "M" in the middle of the serial number) are printed on the unit's rating plate, which is on the left wall of the furnace's interior just above the burner. The rating plate can be found by opening the unit's burner access door, which has slotted openings. Model # Brand & Description ROBF Rheem Classic/Ruud Achiever High Efficiency Upflow Oil Furnace ROPF Rheem Classic/Ruud Achiever High Efficiency Downflow/Horizontal Oil Furnace TZOUP United Refrigeration "Thermal Zone" Upflow Oil Furnace TZODH United Refrigeration "Thermal Zone" Downflow/ Horizontal Oil Furnace

CPSCJan 22, 2009Nationwide• Air Conditioning Division of Rheem Manufacturing Co., of Fort Smith, Ark.

Stryker Craniomaxillofacial Division: Stryker Custom Cranial Implant Kit, small. Distributed b...

Lack of assurance of sterility.

FDAOct 24, 2008Nationwide• Stryker Craniomaxillofacial Division

C. R.Bard, Inc./BardElectrophysiology Division: 7F Bard SSV 13 cm Split Sheath with Valve and sideport Ca...

Failure to insert the guidewire through the introducer needle.

FDAOct 1, 2008Nationwide• C. R.Bard, Inc./BardElectrophysiology Division

Cardinal Health NeuroCare Division: NicoletOne 5.30.2 Software when used with CSeries amplif...

NicoletOne 5.30.2 Software when used with CSeries amplifiers in Fixed Room LTM Configurations with patient room kits. Cardinal Health NeuroCare has confirmed that the 3rd party room relay connected to the A2 wall plate does not always activate if the patient event button connected to the CSeries Amplifier is pressed twice within one second.

FDAJun 13, 2008AL, AR, CA +18 more• Cardinal Health NeuroCare Division

St. Jude Medical Cardiovascular Division: The St. Jude Medical Livewire TC" Ablation Catheter, 8mm ...

St. Jude Medical has initiated a recall of one lot of Livewire TC" Ablation Catheter. The product was mis-labelled as having an 8 mm tip instead of 4 mm tip. This could potentially result in elevated temperatures and formation of coagulum at the tip electrode. If this coagulum were to detach from the product, the worst case this could potentially result in embolization.

FDAJun 5, 2008Nationwide• St. Jude Medical Cardiovascular Division

Cardinal Health NeuroCare Division: NicoletOne photic adapter cable 085-463700

Cardinal Health NeuroCare is implementing a voluntary field correction to replace a quantity of photic adapter cables, part number 085-463700, used to connect the NicLED Photic Strobe option, part number 698-625500, with NicoletOne EEG system. The photic adapter cable has a wiring error which delivers a reduced voltage and results in a decreased intensity of the NicLED photic. This reduced intensi

FDAJun 5, 2008CA, FL, GA +14 more• Cardinal Health NeuroCare Division

Medtronic Heart Valve Division: Hall Easy-Fit Prosthetic Heart Valve - Aortic A7700. Th...

Medtronic has identified an issue with 685 Hall Easy-Fit valves Models A7700 and M7700 in which the holder of the valve was incorrectly secured to the valve. This could potentially make it difficult to easily disengage the holder from the valve.

FDAMar 25, 2008AR, CA, IL +11 more• Medtronic Heart Valve Division

Heraeus Kulzer Inc., Dental Products Division: Heraeus Kulzer GLUMA Comfort Bond + Desensitizer light cu...

The material may solidify in the bottle, and thus be rendered unusable.

FDAJul 9, 2007Nationwide• Heraeus Kulzer Inc., Dental Products Division

Ross Products Division Abbott Laboratories: Embrace Enteral Pump

Continued use of the pump may cause the door pivot point on the back of the pump to crack or break. This will cause the pump to shut down and stop the initiation of enteral feeding.

FDAJun 21, 2007Nationwide• Ross Products Division Abbott Laboratories

Ross Products Division Abbott Laboratories: The Companion ClearStar Pump System, for enteral feeding.

The transducer adapter bracket on the pump could crack or break and potentially result in under delivery of the enteral product.

FDAJun 21, 2007Nationwide• Ross Products Division Abbott Laboratories

Ross Products Division Abbott Laboratories: Patrol enteral pump set with piercing pin, list #520540.

The enteral pump set may have a 1-3 mm slit in the silicone tubing located between the blue connector and the stretch band Safe-T-Valve.

FDAMay 2, 2007Nationwide• Ross Products Division Abbott Laboratories

Stardental Division: Solara Replacement Turbine, Autochuck End Cap, for dental...

End cap component can disassemble.

FDADec 1, 2006Nationwide• Stardental Division

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 1650 Chemistry System, Automated Clinical Chemistry...

Bayer received a customer complaint where the Valproic Acid Quality control material recovered lower than target when it was run in a panel of other Therapeutic Drug (TDM) assays. The under recovery observed by the customer was approximately -25%. Investigation into this issue was initiated promptly following receipt of this complaint.

FDASep 8, 2006PR• Bayer Healthcare, LLC (Diagnostics Division)

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 2400 Chemistry System, Automated Clinical Chemistry...

FDASep 8, 2006PR• Bayer Healthcare, LLC (Diagnostics Division)

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 1200 Chemistry System, Automated Clinical Chemistry...

FDASep 8, 2006PR• Bayer Healthcare, LLC (Diagnostics Division)

Gotham 8-inch APR/APRH Lighting (Gotham) – falling parts (2006)

The recalled lighting fixtures have clear, black, pewter, wheat, umber, gold or champagne gold finishes on the trim. Only models APR incandescent and APRH high-intensity discharge down lights with 8-inch openings are included in this recall.

CPSCAug 15, 2006Nationwide• Gotham Architectural Lighting division of Acuity Lighting Group Inc., of Conyers, Ga.