Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Child Craft Industries, Inc. (Child Craft ceased operations in July of 2009 and sold the "Child Craft" name to Foundations Worldwide Inc., of Medina, Ohio) Foundations Worldwide, Inc. neither manufactured nor sold any of the cribs included in this recall.

Child Craft Industries, Inc. (Child Craft ceased operations in July of 2009 and sold the "Child Craft" name to Foundations Worldwide Inc., of Medina, Ohio) Foundations Worldwide, Inc. neither manufactured nor sold any of the cribs included in this recall. Recalls

All product recalls associated with Child Craft Industries, Inc. (Child Craft ceased operations in July of 2009 and sold the "Child Craft" name to Foundations Worldwide Inc., of Medina, Ohio) Foundations Worldwide, Inc. neither manufactured nor sold any of the cribs included in this recall..

Get alerts for this brand

Recall Summary

Total Recalls

1000

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 2141–2160 of 2399 recalls

Child Craft Drop-Side Cribs (Child Craft) – safety risks (2010)

This recall involves drop-side Child Craft brand cribs using the style of drop-side hardware shown in the pictures. "Child Craft" appears on a label on the crib's frame and identifies the place of manufacture as Salem, Indiana or New Salisbury, Indiana. Cribs: DROP-SIDE CRIBS WITH THE PICTURED HARDWARE MANUFACTURED BETWEEN 2000 and 2009. Model Numbers: F10151 F10171 F10181 F10281 F13311 F13761 F16001 F16011 F16131 F16661 F17001 F17701 F17731 F17801 F17811 F20161 F20181 F20191 F21041 F21081 F21091 F26131 F27301 F27771 F31061 F31701 F32901 F33301 F33601 F33801 F33901 F34101 F35101

CPSCJun 24, 2010Nationwide• Child Craft Industries, Inc. (Child Craft ceased operations in July of 2009 and sold the "Child Craft" name to Foundations Worldwide Inc., of Medina, Ohio) Foundations Worldwide, Inc. neither manufactured nor sold any of the cribs included in this recall.

Harmony High Chairs (Graco) – Fall Risk (2010)

This recall involves all Harmony™ High Chairs. The Harmony™ high chair was manufactured from November 2003 through December 2009 and is no longer in production. The model number can be found on the label that is located on the underside of the foot rest. Harmony™ High Chair Model Numbers 3920BAN 3920BAN2 3920BEB 3920BEBB 3920COV 3920DOH 3920GEI 3920GEIDSP 3920GRN 3920HMP 3920IVY 3920LAU 3920PKR 3930DDH 3930DHO 3935CAL 3935OXB 3935PKR 3935PKRDSP 3935SPM 3935SPMDSP 3935THR 3935THR2 3935THR3 3940BIA 3940BIADSP 3940CAP 3940CLE 3940COT 3940DRM 3940HML 3940MCH 3940NGS 3940SAV 3940SLT 3940SPT 3940STA 3940UNN 3951CLO 3951CLT 3951COT 3951ORC 3951WLO 3955WSR 3960BGN 3960CJG 3960CNP 3960GGG 3980CNR 3E00ABB 3E00BAT 3E00DCF 3E00DCFDSP 3E00DGP 3E00DGPDSP 3E00GPK 3E01BDS 3E01BDSCA 3E01DNY 3E01DNY1 3E01ELP 3E01ELPDSP Note: These model numbers may begin with the letter A, B, C, or D Additional Models: 1752404 1755859 1755860 1757259 1757412 1760429

1...106 107108109 110...120

Page 108 of 120Next

CPSCMar 18, 2010Nationwide• Graco Children's Products Inc., of Atlanta, Ga.

Outdoor Lighting Fixtures – Shock Risk (2010)

This recall involves model AVL outdoor lighting fixtures sold under the American Electric Lighting brand name. The light fixtures are intended for use in parking lots, roadways, commercial environments and office communities. "AVL" is printed on the reflector of each light fixture.

CPSCMar 3, 2010Nationwide• American Electric Lighting, a division of Acuity Brands Lighting Inc., of Conyers, Ga.

Eye Drops Advanced Relief (KC Pharmaceuticals) – Incorrect Labeling (2010)

Labeling: Label Mix-Up: Incorrect back labeling of the immediate container of eye drops (unit carton and front label are correct) which do not list three active ingredients: Dextran 70, PEG 400, and povidone.

Class IIModerate

FDAMar 1, 2010Nationwide• K C Pharmaceuticals Inc

Graco Strollers – Fingertip Amputation Risk (2010)

Laceration Risk

This recall involves Graco Passage™, Alano™ and Spree™ Strollers and Travel Systems with the following model numbers and specific hinge mechanisms: Model Numbers 6303MYC, 6303MYC3 7240DNB, 7240DNB2 7240MKL2, 7240MKL3 7F02GLM3 6320IVY, 6320LAU 7241DDH2, 7241DHO3 7F04TAY3 6330CAP, 6330THR, 6330THR3 7255CLP, 7255CLP2, 7255CRA2, 7255CRA3, 7255CSA3, 7255GPK3, 7255GRN, 7255GRN2, 7255JJB3, 7255ORC2, 7255WLO2, 7255WLO3 7F07EMA3 6F00QIN3, 6F00RRY3 7256CLO2, 7256SPM2, 7256SPM3 7F08DSW3, 7F08LAN3 6F03GLN3 7260BAN, 7260BAN2, 7260BAN3, 7260MRA2, 7260MRA3, 7260PKR, 7260PKR2 7G00DLS3, 7G00DLS4 6G10CSE3 7270BIA, 7270BIA2 7G01CRL3 7235GGA, 7235GGA2 7E01JON2, 7E01JON3 7G04KRA3 7236CDR2 7F00LPE3, 7F00RSH3 7G05GPR3, 7G06WSR3 7237HOL2, 7237HOL3 7F01FOR3 7G07ABB3, 7G07BAT3 Graco manufactured two different styles of hinge mechanisms for these stroller models. Only strollers or travel systems with a plastic, jointed hinge mechanism that has indented canopy positioning notches are included in this recall. The recalled strollers were manufactured between October 2004 and February 2008. The model number and manufacture date are located on the lower inside portion of the rear frame, just above the rear wheels.

CPSCJan 20, 2010Nationwide• Graco Children's Products Inc., of Atlanta, Ga.

Xoran Technologies, Inc.: Xoran MiniCAT CT Scanner ID ENT00001

Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate.

FDADec 14, 2009Nationwide• Xoran Technologies, Inc.

Xoran Technologies, Inc.: Xoran MiniCAT CT Scanner ID ENT00001

Failure of the gantry to rotate. The complaint alleged that the scanner would emit radiation but would not rotate.

Class IIModerate

FDADec 14, 2009Nationwide• Xoran Technologies, Inc.

Monday the Bullfrog Plush Books (Simon & Schuster) – Choking Risk (2009)

Choking Hazard

Monday the Bullfrog is a plush puppet bullfrog with a board book attached to the frog's mouth. It was sold in clear plastic packaging, and the book is marked with ISBN numbers 10: 1416912312 and 13: 9781416912316 printed inside the mouth of the bullfrog.

CPSCDec 9, 2009Nationwide• Simon & Schuster Inc., of New York, N.Y.

Electrolux ICON and Kenmore Pro Gas Ranges – Carbon Monoxide Risk (2009)

Fire/Burn Risk

The following Electrolux ICON and Kenmore PRO 30" free-standing gas range model and serial numbers are included in this recall. For Electrolux ICON, the model and serial numbers are located on the back of the range. For the Kenmore PRO, the model and serial numbers are located near the base of the range just below the bottom right portion of the oven door and also on the back of the range. Not all serial numbers within these ranges are included in the recall. Brand Model Serial Number Range Electrolux ICON Gas Range E30GF74HPS NF83000000 - NF93633000 Kenmore PRO 30" Gas Range 790.79613800 790.79613801

CPSCNov 24, 2009Nationwide• Electrolux Home Products Inc., of Augusta, Ga.

Micromedical Technologies, Inc: AquaStar Water Caloric Irrigator; water caloric stimulato...

Some of the filters on both the display board and the main electronic board (PCB) become oxidized causing the LCD display to be garbled and the timer will not operate.

FDANov 16, 2009Nationwide• Micromedical Technologies, Inc

Churchill Medical Systems, Inc.: Churchill Medical Systems Bag Access Device w/Smartsite N...

Bond between the spike and needle may leak, break or detach resulting in leakage or spillage of chemotherapeutic agents

FDAOct 20, 2009FL• Churchill Medical Systems, Inc.

Roche Diagnostics Operations, Inc.: Roche/Hitachi cobas ONLINE TDM Gentamicin for Roche analy...

A high recovery of the assay may be generated, which would lead to an underdosage of gentamicin being administered to the patient.

FDAOct 7, 2009Nationwide• Roche Diagnostics Operations, Inc.

Roche Diagnostics Operations, Inc.: Roche/Hitachi GENT2 ONLINE TDM Gentamicin for Roche coba...

A high recovery of the assay may be generated, which would lead to an underdosage of gentamicin being administered to the patient.

FDAOct 7, 2009Nationwide• Roche Diagnostics Operations, Inc.

Roche Diagnostics Operations, Inc.: Roche/Hitachi cobas ONLINE TDM Gentamicin for Roche analy...

A high recovery of the assay may be generated, which would lead to an underdosage of gentamicin being administered to the patient.

FDAOct 7, 2009Nationwide• Roche Diagnostics Operations, Inc.

Sequal Technologies Inc: SeQual Technologies Inc. Eclipse Oxygen System, Model 100...

Unit may shut down when operating from the Power Cartridge. A temporary power interruption would cause the unit to sound an alarm and shut down. If the patient does not have access to an alternate supply of oxygen or access to AC or DC power, this may lead to shortness of breath, hypoxia, or in some patients may cause serious health consequences.

FDAOct 1, 2009PR• Sequal Technologies Inc

Cochlear Americas Inc.: Nucleus Non-Magnetic Plug for removable magnet implants, ...

Cochlear implant device component was mis-labeled.

FDASep 30, 2009Nationwide• Cochlear Americas Inc.

Sechrist Industries Inc: Sechrist Hyperbaric Chamber Gurney. The Sechrist Hyperba...

Stryker Medical has received complaints from customers that indicate a bushing in the braking system may fracture, which could result in the brake/steer pedal seizing. If the pedal seizes, the braking system may become inoperable or steering around corners may come more difficult. While no injuries have been associated with these reported events nor has there been reported failure events resulting

FDASep 15, 2009Nationwide• Sechrist Industries Inc

Medical Device Technologies, Inc.: Angiotech Pediatric Bone Marrow Needle. Pediatric Bone M...

Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone Biopsy Needles, Access Needles, Galactography Kit, Stabilization Needles and Needle Guides for packaging integrity.

FDASep 1, 2009Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech Drainage Cather. SKATER Centesis Cather XFr. ...

FDASep 1, 2009Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech Breast Localization Needles: A) Accura BLN an...

FDASep 1, 2009Nationwide• Medical Device Technologies, Inc.