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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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Low RiskFDA Vet
Medical Devices/Monitoring Devices

Smiths Medical ASD Inc.: SurgiVet Advisor Monitor Vital Signs Monitor Systems Recalled for Printing Failure

Agency Publication Date: July 2, 2018
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Summary

Smiths Medical ASD Inc. has recalled 264 SurgiVet Advisor Monitor Vital Signs Monitor Systems, including models V9200P, V9201P, V9204, V9204EU, and V9204UK. These veterinary monitors were recalled because certain printing modes, such as tabular data printing and real-time continuous printouts, may not function properly. This printing defect could lead to incomplete or missing patient records during veterinary procedures. Consumers should contact the manufacturer directly for further instructions regarding this equipment issue.

Risk

The failure of printing modes like real-time continuous printouts and automatic interrupt features prevents the device from generating accurate and timely physical records of vital signs. This can lead to a loss of patient data history, potentially impacting the ability of veterinary staff to review critical trend data during or after medical procedures.

What You Should Do

  1. Identify if your device is affected by checking the model number (V9200P, V9201P, V9204, V9204EU, or V9204UK) and comparing your serial number against the 264 affected units, such as model V9200P serials 4061957, 4066410, and 4055501, or model V9204 serials 4069308, 4058178, and 4065972.
  2. Verify your serial number location on the device's identification label, typically found on the back or bottom of the monitor unit.
  3. Contact Smiths Medical ASD Inc. at their Minneapolis location or through their official customer support channels to discuss the necessary steps for your specific device.
  4. Contact your healthcare provider or the manufacturer for further instructions and potential refund or repair options.
  5. For additional questions, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction regarding printing modes

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: SurgiVet Advisor Monitor Vital Signs Monitor System (Model V9200P)
Model:
V9200P
Lot Numbers:
4061957
4066409
4066410
4055501
4061955
4064238
4067896
4055502
4055503
4060265
4061956
4061958
4061959
4064687
4064688
4065634
4065635
4066411
4067894
4067895
4067897
4069081
Product: SurgiVet Advisor Monitor Vital Signs Monitor System (Model V9201P)
Model:
V9201P
Lot Numbers:
4061521
4061522
4067313
4068755
4068756
4068757
Product: SurgiVet Advisor Monitor Vital Signs Monitor System (Model V9204)
Model:
V9204
Lot Numbers (223):
4069308
4058178
4065972
4061525
4056066
4061638
4068671
4068677
4069554
4069555
4069556
4065971
4056059
4065054
4065055
4065056
4065057
4065058
4065059
4065060
4065061
4065403
4065404
4058146
4065405
4063315
4058145
4061632
4061590
4069051
4069052
4069053
4069054
4056065
4069551
4065398
4065399
4065400
4065401
4065402
4056062
4069309
4062229
4062872
4062881
4064485
4065052
4065053
4065963
4065964
Product: SurgiVet Advisor Monitor Vital Signs Monitor System (Model V9204EU)
Model:
V9204EU
Lot Numbers:
4056096
4056097
4056427
4056428
4056429
4056430
4056431
4056432
4066659
4062871
4062870
Product: SurgiVet Advisor Monitor Vital Signs Monitor System (Model V9204UK)
Model:
V9204UK
Lot Numbers:
4062957
4064505

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 80325
Status: Resolved
Manufacturer: Smiths Medical ASD Inc.
Sold By: military distribution
Manufactured In: United States
Units Affected: 264 devices
Distributed To: Arizona, California, Connecticut, Georgia, Hawaii, Idaho, Illinois, Indiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Pennsylvania, Texas, Virginia, Washington, Wisconsin
Agency Last Updated: August 1, 2018

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