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
/
BioHorizons Implant Systems Inc One Perimeter Park South

BioHorizons Implant Systems Inc One Perimeter Park South Recalls

All product recalls associated with BioHorizons Implant Systems Inc One Perimeter Park South.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16481–16500 of 17592 recalls

BioHorizons Implant Systems Inc One Perimeter Park South: BioHorizons Maximus 3.0 surgical kit, also marketed as Bi...

Dental implants were distributed which lacked the proper instruments for implantation.

FDADec 28, 2005Nationwide• BioHorizons Implant Systems Inc One Perimeter Park South

Acumed LLC: 3.5mm X 32.5mm Cortical Screw used with the Polarus Humer...

Package of 3.5mm X 32.5mm cortical screw may contain 3.5mm X 22.5mm cortical screw.

FDADec 27, 2005AZ, CA, FL +15 more• Acumed LLC

Philips Medical Systems (Cleveland) Inc: Brilliance CT System 6/10/16/16P/40 configuration. No pa...

The system has a gap that can appear between the upper and lower tilt stand covers. The fingers may be squeezed if a person was to place them in this region while the gantry was tilting from an angle to zero tilt angle.

FDA

1...823 824825826 827...880

Page 825 of 880Next

Dec 27, 2005

AZ, CO, GA +16 more

• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Brilliance CT System 6/10/16/16P/40 configuration. No pa...

Class IIModerate

FDADec 27, 2005AZ, CO, GA +16 more• Philips Medical Systems (Cleveland) Inc

Blackstone Medical Inc.: ICON Modular Spinal Fixation System used with the: ICON I...

Pedicle Screw may disengage in post op period requiring intervention

FDADec 23, 2005AL, CA, CO +4 more• Blackstone Medical Inc.

Polaroid DVD Player Batteries (Petters) – Battery Safety Risk (2005)

Fire/Burn Risk

The recall involves external battery packs used with the Polaroid-brand portable DVD players in 7-inch and 8-inch screen sizes. The 7-inch DVD player has model number PDV-0700 and the 8-inch player has a model number of PDV-0800. The players and battery packs are silver in color. The battery packs attach to the bottom of the DVD player and have the following serial numbers: DVD Model Number Battery Pack Serial Number Range PDV-0800 060300020000001 through 060300020018000 070300020008001 through 070300020020000 PDV-0700 04170303070001000001 through 04170303070001005000 04270303070001005001 through 04270303070001010000 05040303070001010001 through 05040303070001014000 05150303070001014101 through 05150303070001016100 05190303070001016101 through 05190303070001020100 05260303070001020101 through 05260303070001024100 06010303070001024401 through 06010303070001024900 060300010024101 through 060300010033523 060300010033524 through 060300010050100 070300010050101 through 070300010114100 080300010114101 through 080300010159100 090300010159101 through 090300010193100

CPSCDec 22, 2005Nationwide• Petters Consumer Brands LLC, of Minnetonka, Minn.

Medtronic Sofamor Danek Instrument Manufacturing: Holt Probe Round Straight

Depth indicators are incorrectly labeled (etched) on a measurement instrument.

FDADec 22, 2005Nationwide• Medtronic Sofamor Danek Instrument Manufacturing

Aspen 3-in-1 Cribs (Graco) – Suffocation Risk (2005)

The recalled cribs are made of wood and have a wooden mattress support. Only cribs with wooden mattress supports and with model number 8740KCW SC and serial number 2803 SC to 1605 are included in this recall. The model and serial number are printed on the envelope attached to the mattress support.

CPSCDec 21, 2005Nationwide• Simplicity Inc., of Reading, Pa. (The firm appears to no longer conduct day to day operations)

Legacy Propane Heaters (Chant) – Potential Safety Issue (2005)

The heaters are propane infrared plaque space heaters sold after September 1, 2005. The units are rectangular in shape and the casing has a white finish. The heaters can be mounted on walls or stand on the floor. The name "Legacy" is centered on the front of the heater immediately below the grill. Affected units have one of the following model numbers: RMC-LI6LP RMC-LI10LP RMC-LI10LPT RMC-LI18LP-F RMC-LI18LPT-F RMC-LI30LP-F RMC-LI30LPT-F The model number is located on the right side panel of the unit. All of the heaters were listed by the Canadian Standards Association.

CPSCDec 20, 2005Nationwide• Chant Kitchen Equipment, of Guandong, China

Bard Access Systems, Inc: Groshong NXT ClearVue 4 Fr Single-Lumen PICC, Bard Access...

Multiple pages in the Instructions For Use booklet were missing print. Booklets were missing either pages 1,4,5,8,9,12,13,and 15, or 2,3,6,7,10,11,14, and 15. These pages contain product description, indications, contraindications, warnings, precautions, possible complications, and insertion instructions.

FDADec 20, 2005Nationwide• Bard Access Systems, Inc

Bard Access Systems, Inc: Groshong NXT 5 Fr. Dual-Lumen Reverse Taper PICC.

FDADec 20, 2005Nationwide• Bard Access Systems, Inc

Chembio Diagnostic System Inc: Sickle-STAT Test Kit, Catalog # SC901, a qualitative test...

Firm received one report of a false negative with the positive control. Internal testing by the firm has shown that the kit lot may result in invalid or false negative interpretations.

FDADec 16, 2005Nationwide• Chembio Diagnostic System Inc

GE Monogram Gas Ranges – Fire Hazard (2005)

Fire/Burn Risk

The recalled GE Monogram built-in ranges include models ZDP48N6RH1SS, ZDP48L6RH1SS, ZDP48N4GH1SS, ZDP48L4GH1SS, ZDP48N6DH1SS, ZDP48L6DH1SS, ZDP36N4DH1SS, and ZDP36L4DH1SS. The recalled ranges have serial numbers starting with DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH. To find the model and serial number, look underneath the top ledge (also called the "bull nose"), above the range controls. They were manufactured from February 1, 2004 to October 1, 2005.

CPSCDec 15, 2005Nationwide• GE Consumer & Industrial, of Louisville, Ky.

Beckman Coulter Inc: COULTER GEN.S Series Hematology Analyzer, PN 6605632, 660...

There is a risk of sample misidentification when processing samples in the Manual aspiration mode.

FDADec 15, 2005Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: COULTER LH 700 Series Hematology Analyzer, PN 6605632 an...

There is a risk of sample misidentification when processing samples in the Manual aspiration mode.

FDADec 15, 2005Nationwide• Beckman Coulter Inc

Little Tree Learning Cubes (Maxim) – Toy Safety Issue (2005)

Choking Hazard

The recalled learning cube is an 8-inch square wooden box with a different activity on each side, including an abacus, blocks with apples and bananas, shapes that can be moved in a zigzag cutout, and a blackboard. The wooden cover has spiral bead maze with wooden beads that slide up, down and around.

CPSCDec 14, 2005Nationwide• Maxim Enterprise Inc., of Lakeville, Mass.

Honda TRX400EX ATVs – Vehicle Safety Concern (2005)

The recall involves Honda 2005 and 2006 model year TRX400EX ATVs. They are adult-sized ATVs designed for use by riders age 16 and older. The 2005 model year ATVs are available in red and yellow. The 2006 model year ATVs are available in red or black. The TRX400EX model name is on the fuel tank and Honda is in white letters on the seat.

CPSCDec 14, 2005Nationwide• American Honda Motor Corp. Inc., of Torrance, Calif.

Custom Ultrasonics, Inc.: 83 plus Mini-flex with accessory crate, Custom Ultrasonic...

The device was marketed without a 510k

FDADec 12, 2005CA, GA, IN +1 more• Custom Ultrasonics, Inc.

Philips Medical Systems North America Co. Phillips: Gyroscan NT MRI System rev 4.x, 5.x, and 6.x software. S...

The Gyroscan NT MRI system has a computer software problem which results in images from one patient being placed into another patient's image record.

FDADec 9, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Smiths Medical MD, Inc.: Large-Volume IV Administration Sets for use with Deltec 3...

Inaccurate infusion rate-administration sets which are used with selected infusion pumps may have a defect which does not allow the pump valve to close completely.

FDADec 8, 2005SC, PR• Smiths Medical MD, Inc.