Bard Access Systems, Inc. recalls
17 recalls filed under Bard Access Systems, Inc.. The most recent was published September 23, 2026.
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Class I · last month
Bard Access Systems, Inc. DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150 recall: this is a downstream recall of class I recall RES 98777
this is a downstream recall of class I recall RES 98777
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Class I · last month
Bard Access Systems, Inc. Power-Trialysis Short-Term Straight Dialysis Catheter recall: this is a downstream recall of class I recall RES 98777
this is a downstream recall of class I recall RES 98777
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Class I · 2 months ago
Bard Access Systems, Inc. BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK recall: After placement of intraosseous (IO) needle sets
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically…
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Class II · 4 months ago
Bard Access Systems, Inc. 5605150 Power-Trialysis Short-Term Straight Dialysis recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. 1174108 PowerPicc Catheter 4 Fr Single-Lumen Udi-Di Code recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. 4380 Economy Soft Tissue Biopsy Tray Udi-Di Code recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. OTP5000 Thora/Para Tray, 5FR recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000662 PowerPicc Solo HF Catheter 5 Fr Triple-Lumen recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. 1274108D PowerPicc SV Catheter 4 Fr Dual-Lumen Rekw2449 recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000525B PowerPicc Provena Solo Catheter 4 Fr Dual-Lumen recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. 5855240 Power-Trialysis Slim-Cath Straight Short-Term recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
About this page
Bard Access Systems, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.