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Regeneration Technologies, Inc.

Regeneration Technologies, Inc. Recalls

All product recalls associated with Regeneration Technologies, Inc..

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

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 3861–3880 of 4099 recalls

Regeneration Technologies, Inc.: Osteofil + RT Allograft Paste in varying sizes. Product ...

The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processing, including sterilization, which has been validated to inactivate and/or remove all viral diseases for which human tissue donors are tested.

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: OPTEFORM RT Moldable Allograft of varying sizes. Produc...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

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Regeneration Technologies, Inc.: Product is REGENAFORM Allograft Moldable Blocks, of varyi...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Product is 1.0cc flowable paste from donor approved for d...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Product is 2.0 cc Opteform RT. Product is labeled in par...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Osteofil Allograft, 5cc. Product is labeled in part: ''...

FDAOct 14, 2005TN• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Osteofil IC Syringeable of varying sizes. Product is lab...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Instrumentation Industries Inc: Flexible Support Arm Assembly. Breathing Tube Support. Ca...

potential for the flexible tube portion of the assembly to become brittle and break

FDAOct 14, 2005FL, IN, NY +1 more• Instrumentation Industries Inc

Regeneration Technologies, Inc.: Osteofil Allograft Paste (Bio) of varying sizes. Product...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: OsteoPack 3 FZ 22cc. Product is labeled in part: ''***P...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Product is RTI Allograft Paste of varying sizes. Product...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Bombardier Outlander 800 ATV – Mechanical Risk (2005)

The recalled vehicles are model year 2006 Outlander 800 H.O. XT Bombardier ATVs. The model numbers affected are 2J6A and 2J6E. The model numbers are located in the serial number on the identification sticker under the seat. The ATVs have the words, "Bombardier" and "Rotax 800" on the fenders.

CPSCOct 11, 2005Nationwide• Bombardier Recreational Products Inc., of Valcourt, Providence of Quebec, Canada

Holiday Time Candle Gift Set (Dan Dee) – Safety Concern (2005)

Fire/Burn Risk

One recalled candle gift set includes three birch bark-covered candles. Each candle measures 3 inches wide but vary in height from 3 to 6 inches. The candles are displayed on a stand with pine cones, cinnamon sticks and red berries. The second recalled candle gift set includes a display stand with three pyramid-shaped candles varying in height from 8 to 12 inches. The candles are either blue with a silver glitter criss-cross pattern or red with a gold glitter criss-cross pattern. Both candle sets were sold under the Holiday Time™ brand name written on the box.

CPSCOct 6, 2005Nationwide• Dan Dee International Ltd., of Jersey City, N.J.

75-Gallon Propane Water Heaters (A.O. Smith) – Safety Hazard (2005)

Fire/Burn Risk

The recall involves 75-gallon propane gas water heaters. The heaters have the name "A.O. Smith," "Reliance," "Apollo," "State," or "Maytag" on the side of the unit. The model number is located on the rating plate. Only units with the model numbers listed below and manufactured between January 2004 and July 2005 are included in the recall. Brand Name Model Number Reliance 675CRRS 675CRRSD S7576PE Apollo A675CQRSL A675CRRSL A675CRRSLCGAD A. O. Smith BT-80-271 FCG-75-271 PCG-75-271 Maytag HRP11275Q State GS675CRRS GS675CRRSD SBS7576PE SBS7576PED SBS7576PECGA SBS7576PECGAD If your unit has one of the model numbers listed above, locate the serial number on the rating plate to determine if it was manufactured between January 2004 and July 2005. If your unit has one of the model numbers listed above, locate the serial number on the rating plate to determine if it was manufactured between January 2004 and July 2005. The serial numbers of units manufactured between January 2004 and July 2005 are listed below. Month/Date of Manufacture Serial Number Begins With: Jan-04 MA04 or AA04 or A04 Feb-04 MB04 or AB04 of B04 Mar-04 MC04 or AC04 or C04 Apr-04 MD04 or AD04 or D04 May-04 ME04 or AE04 or E04 Jun-04 MF04 or AF04 or F04 Jul-04 G04 Aug-04 H04 Sep-04 J04 Oct-04 K04 Nov-04 L04 Dec-04 M04 Jan-05 A05 Feb-05 B05 Mar-05 C05 Apr-05 D05 May-05 E05 Jun-05 F05 Jul-05 G05

CPSCOct 6, 2005Nationwide• A.O. Smith Water Products Co., of Ashland City, Tenn.

Arctic Cat Prowler XT Utility Vehicle – Mechanical Risk (2005)

The Prowler XT was produced in three colors: Green, Cat Green, and Red. The vehicles have the words Arctic Cat on each side of the cargo box, 650 H1 on each side of the front hood, and the name Prowler XT centered on the front of the hood. The recalled units fall within the vehicle identification range (VIN) of 4UF06MPV06T300001 through 4UF06MPV86T300781. Consumers only need to look at the final six digits of the VIN to determine if their vehicle is included in this recall. Model Number of Affected Models Model Model Number Prowler XT Green U2006P2S4BUSG Prowler XT Cat Green U2006P2S4BUSZ Prowler XT Red U2006P2S4BUSR

CPSCSep 22, 2005Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Stanley Vacuum Bottles (PMI) – Potential Defect (2005)

The recall involves the brushed stainless steel and the green 1-liter and 2-quart bottles, and the 24-oz. wide mouth food jar. The recalled thermos bottles have only two spot welds per handle bracket and contain any of the following date code numbers: C 02, D 02, or A 03 The date code is located on the bottom of the bottles just above the "S" and "Y" on the word "STANLEY."

CPSCSep 21, 2005Nationwide• PMI, of Seattle, Wash.

Advanced Sterilization Products: Vaporizer Plate Vaporizer Plate Consumable accessory used...

Fire/Burn Risk

The STERRAD 100 and the STERRAD 100S vaporizer plates are prone to displacement allowing micro-droplets of H2O2 to contact the load. If the vaporizer plate is dislodged, there is an increased chance for operators to have contact with H2O2 resulting in transient burns during the removal of the load.

FDASep 16, 2005Nationwide• Advanced Sterilization Products

Gas Grills (Brinkmann) – Regulator Defect (2005)

Fire/Burn Risk

The recall involves Brinkmann-brand and Charmglow-brand gas grills. The regulator is attached to the side of the grills. Only grills that have regulators with the name "GDA" are affected by this recall. The grills have three to six burners and the name "Brinkmann" or "Charmglow" on the lid.

CPSCSep 13, 2005Nationwide• The Brinkmann Corporation, of Dallas, Texas

Back Trails Jr. Bicycle Helmets (Target) – Safety Issue (2005)

The recall includes Target's "Back Trails Jr." brand toddler, youth and child bicycle helmets sold in various colors. They were manufactured after January 1, 2004. Helmet model numbers: 89888 or 88003 (toddler), 89951 or 88001 (girl's 8-vent youth), 89952 or 88002 (boy's 8-vent youth), or 89917 (14-vent child's) appear on a white label inside the helmets, along with date of manufacture (YYYY/MM/DD) and the words "Made in China." Target product identification numbers: 082-01-0520 (toddler), 082-01-0149 (girl's 8-vent youth), 082-01-0189 (boy's 8-vent youth), and 082-01-0334 (14-vent child's) and the brand name "back trails jr.," appear on the product packaging.

CPSCAug 31, 2005Nationwide• UNA International Limited, of China

Boston Scientific Corporation One Boston: Renegade Hi-Flo Microcatheter Kits, Catalog/Order # 18-29...

Outer box of the product may have an incorrect expiration date listed as 2007-06, while the correct expiration date is 2007-04

FDAAug 10, 2005KY, TX• Boston Scientific Corporation One Boston