How many FDA warning letters has Bard Access Systems, Inc. received?

Argus HQ has not recorded an FDA warning letter for Bard Access Systems, Inc. in our current dataset.

What FDA recalls has Bard Access Systems, Inc. issued?

Argus HQ has recorded 14 FDA recalls tied to Bard Access Systems, Inc..

Is Bard Access Systems, Inc. FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 14 recalls, and 0 approval records for Bard Access Systems, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Bard Access Systems, Inc.

Name: FDA Enforcement Actions Against Bard Access Systems, Inc.
Creator: Argus HQ
License: https://argushq.ai/methodology

Industry: Medical Devices

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOF…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG12…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 008017410…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Tr…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 129…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150…
fda_recall · device_recall2026-07-08
Bard Access Systems, Inc. — Class II recall: CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609…

Frequently asked questions

How many FDA warning letters has Bard Access Systems, Inc. received?: Argus HQ has not recorded an FDA warning letter for Bard Access Systems, Inc. in our current dataset.
What FDA recalls has Bard Access Systems, Inc. issued?: Argus HQ has recorded 14 FDA recalls tied to Bard Access Systems, Inc..
Is Bard Access Systems, Inc. FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 14 recalls, and 0 approval records for Bard Access Systems, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.