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B. Braun Medical, Inc.

B. Braun Medical, Inc. Recalls

All product recalls associated with B. Braun Medical, Inc..

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Recall Summary

Total Recalls

263

Past Year

Class I (Serious)

Most Recent

Oct 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 241–260 of 263 recalls

B. Braun Medical, Inc.: Diapact CRRT Assembled Kit HF/HD with Manifold and Standa...

Faulty tubing does not prime machine as intended.

FDADec 10, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Interventional Systems: Vena Tech LP Vena Cava Filter System, Item No/REF. 050100...

Sterility (package integrity) compromised: package sealing problem leaving packaging being partially open on one of the four sealed Tyvek pouch edges.

FDAOct 30, 2007Nationwide• B. Braun Interventional Systems

The Braun Corporation: Braun wheelchair lift, model NCL, Braun Corporation, Win...

The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

FDAAug 15, 2007

1...11 121314

Page 13 of 14Next

Nationwide

• The Braun Corporation

The Braun Corporation: Braun wheelchair lift, model NVL, Braun Corporation, Win...

The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

FDAAug 15, 2007Nationwide• The Braun Corporation

The Braun Corporation: Braun wheelchair lift, model NL, Braun Corporation, Wina...

The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

FDAAug 15, 2007Nationwide• The Braun Corporation

B. Braun Medical, Inc.: Normal Saline 10ml in 12ml Syringe. The product is shippe...

Particulate matter in product.

FDAJul 30, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Normal Saline 3ml in 12ml Syringe. The product is shipped...

Particulate matter in product.

FDAJul 30, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Thermodilution Right Heart Catheters, Catalog Numbers 604...

Cracks at the Catheter Tip

FDAJun 5, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Ultrasite Horizon Pump IV Set. The product is shipped in ...

Secondary infusion backs up into primary container.

FDAApr 18, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Horizon Pump Metriset Burette Set. The product is shipped...

Secondary infusion backs up into primary container.

FDAApr 18, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: B.Braun HyperFormer Pump Dispensing Set, Catalog Number V...

The integrity of the sterile product barrier may be compromised

FDAApr 11, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: B Braun 9F (O/S) Locking Tearway Introducers non-sterile....

Mislabeled-9F labeled units actually contain 10F devices

FDAMay 8, 2006CT, FL, IN +1 more• B. Braun Medical, Inc.

B. Braun Medical Inc: B. Braun Hyperformer EVA Mixing Container with Hyperforme...

B. Braun Medical has been notified by the manufacturer of the product (Stedim) that a small percentage of the lots leak from the set port when the set port is opened. The leak was identified by Stedim to be due to the incorrect placement of a septum in the set port. The set closure is intact and the leak remains internal until the set port is opened.

FDAFeb 6, 2006Nationwide• B. Braun Medical Inc

B. Braun Medical, Inc.: D-Stat Dry Hemostatic Bandage. The product is an adhesive...

package sealing defect - product may not be sterile

FDASep 15, 2005AZ, CA, FL +13 more• B. Braun Medical, Inc.

B. Braun Medical, Inc.: 7F Locking Tearaway Introducers non-sterile. Part number ...

Tear away sheath assembly may contain a sheath (8FR) that is not the correct French size for the dilator (7FR).

FDASep 1, 2005Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Locking Tear-Away Sheath Introducer Product Line. ACCUG...

Reports that the tearaway introducer sheaths have cracked hubs/handles and/or improper peeling of the sheath during use.

FDAMay 27, 2005IN• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Right Heart Catheter Product Line: Catalog Number 601129...

Reports in a small percentage of Right Heart Catheter Products Line related to cracked catheter tips, leaking at the manifold and cracked hubs.

FDAMay 25, 2005Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Standard and Custom Spinal Trays with 5% Lidocaine Hydroc...

drug ampuls in kits contain particulates

FDAJul 6, 2004Nationwide• B. Braun Medical, Inc.

Braun, B Medical Inc: 18G Catheter is a component in various kits.

Catheter separated from the hub.

FDAApr 16, 2004CA, CO, FL +26 more• Braun, B Medical Inc

Braun, B Medical Inc: Introcan Safety IV Catheter 22G x 1'' PUR with Wings. T...

Mislabeled product. The recalling firm received a complaint that a box of Introcan Safety Catheters, (22G x 1 inch) contained mixed 18G catheters with the same lot number.

FDAMar 19, 2004Nationwide• Braun, B Medical Inc