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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Baxter Healthcare Corporation: PST 500 U Precision Surgical Tables Recalled Due to Unexpected Tabletop Movement

Agency Publication Date: August 6, 2024
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Summary

Baxter Healthcare Corporation is recalling 400 units of the PST 500 U Precision Surgical Table due to a mechanical defect involving loose spring pins in the spindle drives. This defect can cause the tabletop to tilt or shift unexpectedly during use or while being moved, even if the controls are not being touched. This recall affects tables with specific serial numbers distributed across the United States and Canada. Baxter is issuing an Urgent Medical Device Correction to address this safety issue.

Risk

The loose spring pins can cause the surgical table to move or tilt without warning, potentially leading to unintentional patient movement during surgery, preparation, or transport. This poses a significant risk of physical injury to patients undergoing procedures or being moved on the table.

What You Should Do

  1. Identify if your facility has the Baxter PST 500 U Precision Surgical Table by checking for Part Number (Product Code) 4080300 and UDI/DI 00887761973671.
  2. Locate the serial number on your surgical table and compare it against the list of affected units, which includes over 250 specific identifiers such as 107936298, 108028716, 108420763, and 109462925.
  3. Contact Baxter Healthcare Corporation immediately to confirm the status of your equipment and to receive instructions regarding the required Urgent Medical Device Correction.
  4. If you are a healthcare provider using these tables, contact Baxter Healthcare Corporation at 1-800-422-9837 or visit their website at www.baxter.com for detailed technical guidance.
  5. For further information or to report issues, you may also contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Urgent Medical Device Correction

How to: Contact your healthcare provider or the manufacturer (Baxter Healthcare Corporation) for further instructions and potential remedy/refund options.

Affected Products

Product: Baxter PST 500 U, Precision Surgical Table
Model / REF:
4080300
UPC Codes:
00887761973671
Lot Numbers (400):
Serial Numbers: 107936298
107936299
107936300
107946575
107946576
107949857
107951075
107952514
107954982
108021169
108023287
108028575
108028716
108028747
108028798
108028801
108028803
108028817
108028829
108028840
108028846
108029046
108029052
108029053
108049023
108049024
108049948
108049950
108049955
108049967
108050823
108050824
108055575
108055576
108055577
108055581
108123400
108127380
108129826
108129828
108131719
108131745
108133272
108133273
108160433
108160447
108160448
108160452
108160453
108160454

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94944
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Baxter Healthcare Corporation
Manufactured In: United States
Units Affected: 400 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.