Bard Access Systems, Inc. recalls
Every recall we track for Bard Access Systems, Inc. — 40 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Bard Access Systems, Inc. peaked in 2021 (20); 40 since 2017. 3% rated “stop using now”.
All FDA recall records for Bard Access Systems, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 20 | 0 | 20 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 1 | 1 | 1 | 14 | 17 |
Most common reasons for Bard Access Systems, Inc. recalls
What to do if you have a recalled Bard Access Systems, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Bard Access Systems, Inc. recalls
9 shown- UnratedMedical device
Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF:
Bard Access Systems recalls specific DuoGlide short-term dialysis catheters due to a downstream class I recall. Affected models include straight and curved extensions with reference numbers 5625150-5626240. This recall addresses safety concerns from a prior class I recall.
BardAug 10, 2026 - Use cautionMedical device
Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:
Bard recalls specific needle kits for powered drivers due to risk of obturator locking to needle hub, potentially causing delayed therapy during emergency IV access.
BardJul 30, 2026 - UnratedMedical device
Bard Access Systems, Inc. recalls CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr
Bard recalls specific poly midline catheters due to lidocaine ampoules made under deficient manufacturing practices. Affected units have UDI-DI codes 00801741121609 and 00801741108051. Contact Bard for details.
BardMay 21, 2026 - Use cautionMedical device
Bard Access Systems, Inc. recalls BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,
Bard Access Systems recalls 4Fr Single-Lumen PowerPICC Catheters with tubing that may leak, causing discomfort, infection, or other complications. Affected units have specific reference codes and expiration dates.
BardMar 11, 2025 - Use cautionMedical device
Bard Access Systems, Inc. recalls Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/
Bard Access Systems recalls Intraosseous needle kits with potential for needle assembly loss during use. Affected models include D015151NK, D015151MK, and others. Stop using immediately to prevent injury.
Bard Access SystemsJun 20, 2022 - Lower riskMedical device
Bard Access Systems Inc. recalls 5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC
Bard Access Systems recalls 5Fr PowerPICC Catheter kits with incorrect micro-introducers. This could lead to improper catheter placement risks during procedures.
Bard Access SystemsMay 19, 2021 - Lower riskMedical device
Bard Access Systems Inc. recalls 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD
Bard recalls 5 Fr IR PowerPIC: 50cm guidewire in kits labeled for 70cm. This mismatch may cause complications during procedures. Affected units have specific labels and lot numbers.
BardMay 19, 2021 - Lower riskMedical device
Bard Access Systems Inc. recalls REF 7617400, Groshong NXT ClearVue Catheter, intermediate kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741045094 -
Bard Access Systems recalls Groshong NXT ClearVue Catheter intermediate kits due to connector problems that may prevent catheter insertion. Affected units have specific UDI codes and lot numbers.
Bard Access SystemsApr 7, 2021 - Lower riskMedical device
Bard Access Systems Inc. recalls PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray with Tyvek lid within
Bard Access Systems recalls PowerPICC Provena Catheters (3 Fr. Single lumen and 4 Fr. Dual Lumen) due to possible leaks at the luer hub extension leg junction. Product codes and serial numbers listed in the recall.
Bard Access SystemsDec 28, 2017
Bard Access Systems, Inc. recall questions
How many recalls has Bard Access Systems, Inc. had?
40 recalls from Bard Access Systems, Inc. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Bard Access Systems, Inc. recall?
Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF:, dated Aug 10, 2026. Every Bard Access Systems, Inc. recall is listed on this page, newest first.
Why are Bard Access Systems, Inc. products recalled?
The most common reasons on record: this is a downstream recall of class I recall RES 98777 (2).
What should I do if I have a recalled Bard Access Systems, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Bard Access Systems, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.