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Baxter Healthcare Corp. Rt

Baxter Healthcare Corp. Rt Recalls

All product recalls associated with Baxter Healthcare Corp. Rt.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

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 7581–7600 of 7756 recalls

Baxter Healthcare Corp. Rt: Clearlink System Vented Paclitaxel Set, 10 drops/mL, 111'...

There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process.

FDAJul 16, 2003Nationwide• Baxter Healthcare Corp. Rt

Blue Torch Medical Technologies: CaverMap Surgical Aid Disposable Kit with Focused Probe T...

Product's sterility is compromised due to a failed sterility audit

FDAJul 10, 2003NY, TX• Blue Torch Medical Technologies

Boston Scientific Corporation: ASAP Channel Cut Biopsy System, 14 gauge Reference Number...

Sterility of the device may be compromised due to a lack of package integrity

FDAJul 3, 2003Nationwide

1...378 379380381 382...388

Page 380 of 388Next

• Boston Scientific Corporation

Rear Projection TVs (Toshiba) – Model Safety Concern (2003)

Laceration Risk

This program includes a limited number of units of the following Toshiba rear projection televisions: Model 50A62, Model 51H83, and Model 57H83. To determine if your television set is affected by this corrective action, go to www.tacp.toshiba.com/safety_notice.asp and follow the instructions.

CPSCJul 3, 2003Nationwide• Toshiba America Consumer Products, Inc., of Wayne, N.J.

Boston Scientific Corporation: Wallstent Enteral Endoprothesis with Unistep Plus Deliver...

Mislabeled: Product is labeled as a 20 mm X 90 mm, but is actually a 22 mm X 60 mm

FDAJun 26, 2003CO, FL, IL +4 more• Boston Scientific Corporation

Ski-Doo Snowmobiles (Bombardier) – Vehicle Safety Issue (2003)

Laceration Risk

The recalled snowmobiles are 2-tone blue or all black. The name of the engine is written on the hood: Rotax 4-TEC V-1000 or Rotax 2-TEC 800 SDI.

CPSCJun 24, 2003Nationwide• Bombardier Motor Corporation of America, of Grant, Fla.

Boston Scientific Corporation: Fibered Platinum Coil, 0.035 Type, 4 mm x 30 mm Catalog...

Product 's Outer box label may not match pouch label: a 4mm x 30 mm coil may be labeled as a 9 mm x 60 mm or vice versa

FDAJun 23, 2003Nationwide• Boston Scientific Corporation

Beckman Coulter Inc: Power Processor Aliquot Tube Labels Part 800255

Labels are missing an expiration date and storage instructions, increasing the likelihood that they will not be used by the expiration date or may be stored under conditions that would cause adhesive failure and loss of identity of sample or aliquot during testing.

FDAJun 23, 2003Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Synchron LX Systems Primary Tube Sample Template (a piec...

Dead volume on sight gauge for the Synchron LX 20 and LX 20 Pro Systems not stated, which may result in instrument error.

FDAJun 19, 2003Nationwide• Beckman Coulter Inc

Bayer HealthCare LLC, Diagnostics Div: Clinitek 50 Urine Chemistry Analyzer; Product codes 6509C...

Analyzer will produce erroneous results due to missing grounding strap.

FDAJun 19, 2003Nationwide• Bayer HealthCare LLC, Diagnostics Div

Beckman Coulter Inc: Access Immunoassay System Technical Update 03.1, Part num...

Defective software media distributed with upgrade software may cause installation failure and systems lock.

FDAJun 18, 2003Nationwide• Beckman Coulter Inc

Ballard Medical Products: Kimberly-Clark / Ballard TRACH-CARE* MAC (Multi Access Ca...

Incorrect plug was included in the multi access catheter pkg. When inserted in the 'Y' it may disengage, allowing a leak of ventilator gases.

FDAJun 13, 2003Nationwide• Ballard Medical Products

Abbott Laboratories HPD/ADD: AxSYM AFP Reagent Pack, list 7A48-22 (100 test kit), 7A48...

AFP results obtained when using the 1:101 automated dilution protocol showed an overestimation of AFP of up to 30.5%

FDAJun 12, 2003Nationwide• Abbott Laboratories HPD/ADD