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BA Sweetie Candy Co

BA Sweetie Candy Co Recalls

All product recalls associated with BA Sweetie Candy Co.

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Recall Summary

Total Recalls

350

Past Year

Class I (Serious)

Most Recent

Nov 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 350 recalls

Sugar Free Chocolate Bridge Mix (BA Sweetie) – Peanut Contamination (2009)

Salmonella

Product is being recalled because it was manufactured using peanut products recalled by Peanut Corporation of America. The peanut products has the potential to be contaminated with Salmonella

Class IHigh

FDAFeb 3, 2009IN, OH• BA Sweetie Candy Co

BA Sweetie Double Dip Peanuts (BA Sweetie) – Peanut Contamination (2009)

Salmonella

Product is being recalled because it was manufactured using peanut products recalled by Peanut Corporation of America. The peanut products has the potential to be contaminated with Salmonella

Class IHigh

FDAFeb 3, 2009IN, OH• BA Sweetie Candy Co

BA Sweetie Chocolate Bridge Mix (BA Sweetie) – Peanut Contamination (2009)

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Salmonella

Product is being recalled because it was manufactured using peanut products recalled by Peanut Corporation of America. The peanut products has the potential to be contaminated with Salmonella

Class IHigh

FDAFeb 3, 2009IN, OH• BA Sweetie Candy Co

Sugar Free Chocolate Peanuts (BA Sweetie) – Peanut Contamination (2009)

Salmonella

Product is being recalled because it was manufactured using peanut products recalled by Peanut Corporation of America. The peanut products has the potential to be contaminated with Salmonella

Class IHigh

FDAFeb 3, 2009IN, OH• BA Sweetie Candy Co

Spectranetics Corporation: Spectranetics SLS II 14Fr. Laser Sheath Kit, REF 500-012,...

Catheter pouch was mislabeled with the wrong size.

FDAOct 15, 2008CA, FL, MI +6 more• Spectranetics Corporation

Spectranetics Corporation: Turbo Elite 0.9mm Turbo Elite (TE) RX, Model #410-154, ti...

The catheter pouch label was incorrectly labeled with the wrong size.

FDAJul 4, 2008Nationwide• Spectranetics Corporation

Spectranetics Corporation: Spectranetics Quick-Cross Support Catheters, .035in x 90c...

Mislabeling: Catheters were placed into mis-labeled inner pouches as REF Number 518-037, 135 cm--the exterior box labeling is correct as 90 cm.

FDADec 10, 2007Nationwide• Spectranetics Corporation

Haemonetics Corporation: Haemonetics cardioPAT System, Product List Number 02050, ...

Labeling (additional) use instructions: to clarify proper position of cardioPAT device and post-op line to prevent fluid build up from patient's chest

FDAOct 15, 2007Nationwide• Haemonetics Corporation

Fruit Slicer (Farberware) – Laceration Hazard (2006)

Laceration Risk

The recalled product is the Farberware® Classic Series™ Fruit Slicer and Corer with model number 78350. The model number is written on the packaging. The fruit slicer/corer is an eight-section round metal blade encircled in hard black plastic with two handles. "FARBERWARE" is printed on the top of the handle.

CPSCDec 19, 2006Nationwide• Lifetime Brands Inc., of Westbury, N.Y.

Discount Diabetic Supply: One Touch Ultra Blood Glucose test strips, LifeScan, a J...

Counterfeit-blood glucose test strips (manufacturer unknown)

FDAOct 19, 2006Nationwide• Discount Diabetic Supply

Southern Prosthetic Supply Co.: SPS Blue Line Tube Clamp Adapters, Product No. BL120M

Device Fracturing: recent design and process changes leave the device susceptible to fracturing, which could cause the prosthesis to fail

FDAOct 3, 2006Nationwide• Southern Prosthetic Supply Co.

Haemonetics Corporation: SmartSuction Harmony Powered Suction Device Model Number:...

Faulty circuit board may short circuit and cause electric shock to operator

FDAJul 28, 2006AZ, CT, GA +2 more• Haemonetics Corporation

LYCKSELE Chair Bed (IKEA) – Fingertip Amputation Risk (2006)

Laceration Risk

This recall involves LYCKSELE chair beds and sofa beds produced before July 2005 and date stamped (year/week) 0526 and earlier. The frames are constructed of iron and have natural wood slats. IKEA, the article number (700-326-82 chair bed and 900-326-81 sofa bed) and a four-digit date stamp printed on a white sticker located on the underside of the product.

CPSCJul 19, 2006Nationwide• IKEA Home Furnishings, of Plymouth Meeting, Pa.

Outdoor Candles (IKEA) – Fire and Burn Risk (2006)

Fire/Burn Risk

The recall involves the ANGAR (#200.301.24) and SAMLAS (#900.524.43) outdoor candles. The candle's container is made of silver-colored metal and measures about four inches wide by two inches high. The container is filled with white wax. The candle's wick is about ½ inch square and is made of brown fiberboard. They were sold in packages of six candles. The candle name and article number (#) is written on the instructions for use accompanying the candles.

CPSCMay 18, 2006Nationwide• IKEA Home Furnishings, of Plymouth Meeting, Pa.

Kinetic Concepts, Inc: Sterile packaged wound dressing with white and green inne...

Complaints received regarding difficulty opening the nonadherent layer of the device prior to application to open abdominal wounds.

FDAMar 17, 2006Nationwide• Kinetic Concepts, Inc

Youth Hooded Fleece (Next Marketing) – Strangulation Risk (2006)

The recalled youth hooded fleece garments have drawstrings. They were sold in a variety of colors and many of them have the names of colleges and universities printed or embroidered on them. A sewn-in tag reads, "Lil Fan" or "LF 2."

CPSCFeb 24, 2006Nationwide• Next Marketing Inc., of Wabash, Ind.

Haemonetics Corporation: Haemonetics Cell Saver 5 Autogolous Blood Recovery System...

Device emits radiofrequency which exceed the IEC 60601-1-2 International Standard

FDADec 21, 2005Nationwide• Haemonetics Corporation

Pulmonetic Systems, Inc.: Lap Top Ventilator (LTV) Series continuous ventilator, mo...

Pulmonetic Systems has identified the potential of a printed circuit board malfunction, which can result in a ventilator malfunctio (e.g. Vent INOP, HW Fault, Xducer Fault) and possibly resulting in failure of the ventilator to breathe for the patient. This malfunction may occur without an accompanying audible alarm.

FDANov 9, 2005AK, AZ, CA +22 more• Pulmonetic Systems, Inc.

Kinetic Concepts, Inc: V.A.C. ATS Canister with Gel (500 mL), Part #M6275063/10....

Possible mislabeling of shipping cartons.

FDASep 16, 2005Nationwide• Kinetic Concepts, Inc

Sesame Street Sunglasses (American Greetings) – Safety Risk (2005)

Choking Hazard

This recall involves DesignWare® child-size sunglasses with Sesame Street character decals. Sold in quantities of four, each package contains a yellow, blue, red and green pair of sunglasses. The bright green cardboard backer has the Sesame Street and DesignWare® logo on the front, and model number SUN-1219 on the back.

CPSCSep 1, 2005Nationwide• American Greetings Corp., of Cleveland, Ohio