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Boston Scientific Corporation

Boston Scientific Corporation Recalls

All product recalls associated with Boston Scientific Corporation.

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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 35061–35080 of 37665 recalls

Boston Scientific Corporation: Precision Tack Transvaginal Sling Kit with Non-Absorbable...

Sterility of device compromised due to breach in packaging

FDAOct 25, 2005Nationwide• Boston Scientific Corporation

Boston Scientific Corporation: TLC Retractor and Single Step Pelvic Drape (contains 1 P...

Sterility of device compromised due to breach in packaging

FDAOct 25, 2005Nationwide• Boston Scientific Corporation

Boston Scientific Corporation: Capio CL Kit Transvaginal Suture Capturing Device (1TLC...

Sterility of device compromised due to breach in packaging

FDAOct 25, 2005Nationwide• Boston Scientific Corporation

1...1752 175317541755 1756...1884

Page 1754 of 1884Next

Ossur Grjothals 5 Reykjavik Ireland: Elation, Class I Medical Device Prosthetic product, Compo...

After one year devices assembled with a new type of O-rings could exhibit enough wear to allow a gradual oil leak which would increase play in the ankle sub-assembly of the foot.

FDAOct 21, 2005Nationwide• Ossur Grjothals 5 Reykjavik Ireland

Merit Medical Systems, Inc: Viceroy Inflation Syringe, 60mL, Sterile, Rx only.

Inflation device may not hold vacuum during angioplasty procedure.

FDAOct 21, 2005FL, OR, UT• Merit Medical Systems, Inc

Musical Bells Christmas Trees (Cracker Barrel) – defective item (2005)

Fire/Burn Risk

These battery-operated Miniature Musical Bells Christmas Trees have the item number 233010. The tree is about 18 inches high and 8 inches wide with three tiers of bells and a lighted star at the top. Each tree has "Made in China" embossed on the bottom. The trees use eight "AA" 1.5-volt batteries.

CPSCOct 20, 2005Nationwide• Cracker Barrel Old Country Store®, of Lebanon, Tenn.

In-Wall Volume Controls (Dana Innovations) – installation risk (2005)

Fire/Burn Risk

Sold under the brand names Architectural Audio and HomeTech, these in-wall volume controls were professionally installed as part of whole house audio systems. The switch plate covers for the recalled systems are white or almond, and "aVc" (amplified volume control) is imprinted above the volume control. They have the following model numbers: Brand Model Numbers Architectural Audio 20127 20128 HomeTech 10114 10115 The model number is not visible to the consumer, and consumers are instructed not to remove the keypads from the wall to look for a model number. All serial numbers are included in the recall.

CPSCOct 20, 2005Nationwide• Dana Innovations, of San Clemente, Calif.

Gas-Packs (International Comfort) – heating malfunction (2005)

The recall involves certain limited "Gas-Packs" sold under the brand names Airquest, Arcoaire, Comfortmaker, Heil, Keeprite, Kenmore, ICP Commercial, and Tempstar. The affected units were manufactured between the 41st week of 2000 and the 26th week of 2003, and are installed outside the home. The model and serial numbers of affected units are printed on the unit's rating plate, as shown in the photo. Model numbers appear in the following typical format: PGC036K060A; serial numbers appear in the following typical format: L004112345. Affected models begin with PGC, PGF, PGS, GPFM, GPSM, or GPCM. Please contact the ICP phone number with the complete model and serial number from your unit, or visit www.icpusa.com, for assistance in determining whether your unit is covered.

CPSCOct 19, 2005Nationwide• International Comfort Products LLC, of Lewisburg, Tenn.

Terumo Cardiovascular Systems Corp: Terumo Sarns brand Soft-Flow Aortic Cannula with flange, ...

The product is labeled as sterile, but the firm has determined that the suture flange may tear through the front of the package.

FDAOct 19, 2005CA, IN, MO• Terumo Cardiovascular Systems Corp

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

While on battery power, the system may flash a low battery warning even though the battery is adequately charged.

FDAOct 19, 2005Nationwide• Terumo Cardiovascular Systems Corp

Jumbo Pencils with Sharpeners (Target) – Potential Safety Issue (2005)

Laceration Risk

The jumbo pencil has a red eraser on the end and comes with a pencil sharpener. Pencils are either short, 8 ½ inches long and one inch wide, or long, 15 inches long and ½ inch wide. The pencils are blue, red or striped. The sharpeners are pink or blue and come in a clear plastic pouch. Model number 70505 is printed on the pouch.

CPSCOct 18, 2005Nationwide• Target Corp., of Minneapolis, Minn.

Child Craft Cribs – structural defect (2005)

Laceration Risk

The recalled cribs have their model number 37001 or 27601 printed on a label on the bottom rail of the head or foot board. The 37001 crib comes in three finishes: chestnut, white and cherry. The 27601 crib in aspen also comes in three finishes: natural, pecan and cognac.

CPSCOct 18, 2005Nationwide• Child Craft Industries Inc., of New Salisbury, Ind.

Stihl Backpack Blowers – mechanical issue (2005)

These backpack blowers have serial numbers ranging from 264264925 through 264740832 which are located on top of the engine's cylinder on the fin. The spark plug boot can be removed to view the serial number from the exterior of the blower.

CPSCOct 18, 2005Nationwide• Stihl Inc. of Virginia Beach, Va.

Abbott Laboratories MPG: ARCHITECT STAT Myoglobin Calibrators; list 02K43-01; each...

Some of the kits were shipped at the incorrect shipping temperature. They were shipped ambient, but should have been shipped frozen.

FDAOct 17, 2005KY, MT, PA +2 more• Abbott Laboratories MPG

Kelty Speedster Jogging Stroller – Safety Concern (2005)

The recalled stroller has an aluminum frame and a cloth seat, with a sun canopy. The recalled stroller has model number 20050016 and serial numbers: S1000001D0504 through S1000800D0504 and S1000001D0506 through S1000200D0506. Each stroller has a tag, located inside the child's seat compartment, which lists the model name and number. A sticker on the rear frame lists the serial number. There are two yellow handle-locking clips, one on each side of the stroller frame that secures the handle from movement.

CPSCOct 14, 2005Nationwide• Kelty Division of American Recreation Products Inc., of Boulder, Colo.

Polaris Snowmobiles – Potential Mechanical Failure (2005)

Fire/Burn Risk

The recall involves all model year 2005 900 Fusion, 900 RMK, 900 Switchback snowmobiles, and select model year 2006 600HO Fusion / RMK / Switchback, 900 Fusion / RMK / Switchback, FS Classic / Touring, and FST Classic / Touring / Switchback snowmobiles. The model and serial number (VIN) identification decal is located on the right side of the tunnel underneath the seat. See affected model table below. Model Number of Affected Snowmobiles: Model Model Number 2005 900 Fusion S05MP8DS (A)(B)(C) 2005 900 RMK S05PL8DS (A)(B)(C)(D) S05PM8DS (A)(B) S05PN8DS S05PN8DE 2005 900 Switchback S05PS8DS 2006 600 HO Fusion S06MP6FS (A)(B) S06MC6FS S06ME6FS 2006 600 HO RMK S06PK6FS (A) 2006 600 HO Switchback S06PS6FS (A) 2006 900 Fusion S06MP8DS (A)(B) 2006 900 RMK S06PL8DS (A)(B) S06PM8DS (A) S06PN8DS (A) S06PR8DS 2006 900 Switchback S06PS8DS (A) 2006 FS Classic S06PD7ES 2006 FS Touring S06PT7ES 2006 FST Classic S06PD7FS 2006 FST Touring S06PT7FS 2006 FST Switchback S06PS7FS

CPSCOct 14, 2005Nationwide• Polaris Industries Inc., of Medina, Minn.

Regeneration Technologies, Inc.: Product is 1.0 cc Regenaform RT. Product is labeled in...

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.: Osteofil ICM Moldable Strip of varying sizes. Product is...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Osteofil + RT Allograft Paste 10cc. Product is labeled ...

FDAOct 14, 2005TN• Regeneration Technologies, Inc.

Regeneration Technologies, Inc.: Product is REGENAFIL Allograft Paste, Syringe, 0.5cc. Pr...

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.