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Beco Baby Carrier Inc., of Newport Beach, Calif.

Beco Baby Carrier Inc., of Newport Beach, Calif. Recalls

All product recalls associated with Beco Baby Carrier Inc., of Newport Beach, Calif..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 33001–33020 of 37665 recalls

Beco Butterfly Baby Carriers – Safety Concern (2008)

The recalled infant carriers were sold under brand name "Beco Baby Carrier Butterfly." The carriers have a black label with a green "b" logo on the left side and a butterfly on the right side. The label is sewn on the outside of the carrier. The following carrier styles are included in the recall: Mia, Pony Express, Carnival, Addison, Ethan, Sophia, Cameron, Ava and Joshua.

CPSCApr 22, 2008Nationwide• Beco Baby Carrier Inc., of Newport Beach, Calif.

Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342: OMG (Observational Mechanical Gateway) Connector - A Mode...

The recall was initiated because there is a possibility that the OMG Connector-A is incorrectly packaged with an OMG Connector-M Instruction manual.

FDAApr 22, 2008Nationwide• Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342

Mentor Texas, Inc: Contour Genesis Aspiration Tubing, 12'; Part Number CG-PT...

1...1649 165016511652 1653...1884

Page 1651 of 1884Next

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Contour Genesis Inf/IR Tubing; Part Number CG-UT; distrib...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Lamis Tubing Set, 9'; 10/box; Part Number LAM-TUBING; dis...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Psi-Tec Syringe Pump Infiltration Tubing, 10'; 10/box; Pa...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Psi-Tec Tubing, 12'; 10/box; Part Number PT-5558; distrib...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Y Tubing Set, 9'; 10/box; Part Number LAM-Y; distributed ...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Irrigation Tubing, 25'; Part Number 5120-25; distributed ...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Autofuse Tubing, DIS SI; Part Number AFTU-DS; distributed...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Hi-Vac Tubing, 8'; 10/box; Part Number B-5558; distribute...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Mentor Texas, Inc: Contour Genesis Infiltration Tubing, 13'; Part Number CG-...

During packaging integrity validation, it was found that various product packages could fail, compromising the sterility of the devices.

FDAApr 21, 2008PR• Mentor Texas, Inc

Intuitive Surgical, Inc.: INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODE; S Card...

The product has a software interface problem. When the product is connected to the da Vinci IS2000 System it will not allow the System to recognize the Instrument which makes the IS2000 CPG instrument nonfunctional at all sites. Risks associated are loss of operability of the instrument, delay in surgery, and loss of dexterity.

FDAApr 18, 2008Nationwide• Intuitive Surgical, Inc.

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

The power supply may fail to charge the batteries due to various hardware malfunctions.

FDAApr 17, 2008Nationwide• Terumo Cardiovascular Systems Corporation

Sunquest Information Systems, Inc.: Sunquest Laboratory versions 5.3, 5.4, 6.1, 6.2 and 6.3. ...

Sunquest has identified a problem with IGO interfaces when performing an Online File Cleanup (OFC) that can lead to the test results of one patient filing to another patient when the order codes are the same. Performing an OFC prior to all results being assigned an accession number may cause the patient results to remain in a temporary file where they can be incorrectly associated to the wrong pat

FDAApr 17, 2008Nationwide• Sunquest Information Systems, Inc.

Biomet Sports Medicine: BIOMET EZLoc 9-10mm TM Femoral Fixation, Catalog Number ...

This recall was initiated following an investigation which identified that: EZLoc Femoral Fixation devices, from two finished good lots were distributed with the incorrect component size inside the package. As supplied, label indicates product size as EZLoc 7-8mm 904780 L305240. Actual product enclosed may be EZLoc 9-10mm. Alternatively, as supplied, label indicates product size as EZLoc 9-1

FDAApr 17, 2008Nationwide• Biomet Sports Medicine

Biomet Sports Medicine: BIOMET EZLoc 7-8mm TM Femoral Fixation, Catalog Number 90...

This recall was initiated following an investigation which identified that: EZLoc Femoral Fixation devices, from two finished good lots were distributed with the incorrect component size inside the package. As supplied, label indicates product size as EZLoc 7-8mm 904780 L305240. Actual product enclosed may be EZLoc 9-10mm. Alternatively, as supplied, label indicates product size as EZLoc 9-1

FDAApr 17, 2008Nationwide• Biomet Sports Medicine

Abbott Spine: PathFinder Cannulated T-Handle Bone Awl, Part Number 1155...

Breakage - Tips on the Pathfinder Bone Awl may bend or break prematurely. The firm has received internal non-conformances and complaints where the tips of the Awl were worn and damaged. Of the tip breaks, six have had material missing. During the same period, there were 15 complaints reported where the tip broke off at the weld after repeated use (1-3 years). The firm found several possible ca

FDAApr 17, 2008AZ, AR, CA +19 more• Abbott Spine

OEC Medical Systems, Inc: OEC 9800 Image Intensified fluoroscopic x-ray system (inc...

Use of existing four-pedal footswitch on a different machine may cause various operational errors.

FDAApr 15, 2008Nationwide• OEC Medical Systems, Inc

Merit Medical Systems, Inc.: Custom Kit, REF: K05-00843, Revision L, Sterile, Merit M...

Convenience kits may be non-sterile due to inadequate package sealing.

FDAApr 15, 2008MO, OR• Merit Medical Systems, Inc.