Public recall detail

Needle Kit For Powered Driver

2026-08-04

medium
Health products Health product recall
Quick summary

Quick summary: Needle Kit For Powered Driver. Reason: Health product recall. Category: Health products. Date: 2026-08-04.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Needle Kit For Powered Driver. Reason: Health product recall. Category: Health products. Date: 2026-08-04.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandBard Access Systems, Inc.
ProductNeedle Kit For Powered Driver
IssueMedical devices - Performance
Recall classType I
IdentificationRA-82427

Affected products

ProductNeedle Kit For Powered Driver
LotBSLC10105
ModelD015251NK
Serial numberBSLC10105
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC12123
ModelD015251NK
Serial numberBSLC12123
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC9485
ModelD015351NK
Serial numberBSLC9485
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC10874
ModelD015351NK
Serial numberBSLC10874
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC10101
ModelD015451NK
Serial numberBSLC10101
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC10520
ModelD015451NK
Serial numberBSLC10520
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC9465
ModelD015551NK
Serial numberBSLC9465
DescriptionNeedle Kit For Powered Driver
ProductNeedle Kit For Powered Driver
LotBSLC11452
ModelD015551NK
Serial numberBSLC11452
DescriptionNeedle Kit For Powered Driver

Issue

Some lots were manufactured with out-of- tolerance dimensions, and as a result some users have reported difficulty removing the obturator (stylet) following placement of the BD Intraosseous Vascular Access System Needle Sets. Based on complaint reports, bench testing completed by BD and clinical observations, this may occur when pulling back on the drill during the insertion or when failing to pull straight back with the powered driver or incorrectly rotating or trying to unscrew the obturator. These actions allow the rotation and locking of the obturator-needle hub interface for specific lots of the product with out-of-tolerance dimensions.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesBard Access Systems, Inc.605 North 5600 West, Salt Lake City, Utah, United States, 84116
Recall date2026-07-30
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-82427
Background{}
CompaniesBard Access Systems, Inc.605 North 5600 West, Salt Lake City, Utah, United States, 84116
AudiencesHealthcare
Source updated2026-08-04

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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