BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
- Agency
- FDA Drug
- Recall date
- Jul 9, 2026
- Status
- Ongoing
- Company
- CareFusion 213, LLC
1. What product was recalled?
BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0
BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31
Quantity: 43,066,599 units
Code or lot text: Lots: 4062535, 4065201, 4066446, Exp. 2/28/2027; 4141090, Exp. 5/31/2027; 4180288, 4197695, 4197697, 4180291, Exp. 6/30/2027; 4219454, 4221945, 4221966, 4222853, 4224361, Exp. 7/31/2027; 4228482, 4248656, 4249026, 4248961, 4249818, 4250729, Exp. 8/31/2027; 5124984, 5127231, 5129058, 5126398, 5129488, Exp. 4/30/2028; 5130576, 5142947, 5147432, 5154673, 5154671, 5156442, 5157968, 5158031, 5150160, 5155824, Exp. 5/31/2028; 5176326, 5181676, 5181074, 5182660, 5188102, 5188103, Exp. 6/30/2028; 5195818, 5199118, 5209474, 5210853, 5211985, 5211907, 5211212, Exp. 7/31/2028; 5226576, 5227151, 5230531, 5241733, 5242057, 5243430, 5246952, 5248375, 5248189, Exp. 8/31/2028; 5254509, 5274692, 5276968, 5279226, 5280240, Exp. 9/30/2028; 5305661, 5307185, 5309623, 5310701, Exp. 10/31/2028; 5346128, 5350797, Exp. 12/31/2028; 6031034, 6031234, 6037918, Exp. 1/31/2029; 6051588, 6054213, 6062168, 6063361, Exp. 2/28/2029; 6069891, Exp. 3/31/2029; 6111107, Exp. 4/30/2029.
- LOT
- 4065201
- LOT
- 4066446
- LOT
- 4141090
- LOT
- 4180288
- LOT
- 4180291
- LOT
- 4197695
- LOT
- 4197697
- LOT
- 4219454
- LOT
- 4221945
- LOT
- 4221966
- LOT
- 4222853
- LOT
- 4224361
- LOT
- 4228482
- LOT
- 4248656
- LOT
- 4248961
- LOT
- 4249026
- LOT
- 4249818
- LOT
- 4250729
- LOT
- 5124984
- LOT
- 5126398
- LOT
- 5127231
- LOT
- 5129058
- LOT
- 5129488
- LOT
- 5130576
- LOT
- 5142947
- LOT
- 5147432
- LOT
- 5150160
- LOT
- 5154671
- LOT
- 5154673
- LOT
- 5155824
- LOT
- 5156442
- LOT
- 5157968
- LOT
- 5158031
- LOT
- 5176326
- LOT
- 5181074
- LOT
- 5181676
- LOT
- 5182660
- LOT
- 5188102
- LOT
- 5188103
- LOT
- 5195818
- LOT
- 5199118
- LOT
- 5209474
- LOT
- 5210853
- LOT
- 5211212
- LOT
- 5211907
- LOT
- 5211985
- LOT
- 5226576
- LOT
- 5227151
- LOT
- 5230531
- LOT
- 5241733
- LOT
- 5242057
- LOT
- 5243430
- LOT
- 5246952
- LOT
- 5248189
- LOT
- 5248375
- LOT
- 5254509
- LOT
- 5274692
- LOT
- 5276968
- LOT
- 5279226
- LOT
- 5280240
- LOT
- 5305661
- LOT
- 5307185
- LOT
- 5309623
- LOT
- 5310701
- LOT
- 5346128
- LOT
- 5350797
- LOT
- 6031034
- LOT
- 6031234
- LOT
- 6037918
- LOT
- 6051588
- LOT
- 6054213
- LOT
- 6062168
- LOT
- 6063361
- LOT
- 6069891
- LOT
- 6111107
- LOT
- Exp. 1/31/2029
- LOT
- Exp. 10/31/2028
- LOT
- Exp. 12/31/2028
- LOT
- Exp. 2/28/2027
- LOT
- Exp. 2/28/2029
- LOT
- Exp. 3/31/2029
- LOT
- Exp. 4/30/2028
- LOT
- Exp. 4/30/2029.
- LOT
- Exp. 5/31/2027
- LOT
- Exp. 5/31/2028
- LOT
- Exp. 6/30/2027
- LOT
- Exp. 6/30/2028
- LOT
- Exp. 7/31/2027
- LOT
- Exp. 7/31/2028
- LOT
- Exp. 8/31/2027
- LOT
- Exp. 8/31/2028
- LOT
- Exp. 9/30/2028
- LOT
- Lots: 4062535
- NDC
- 54365-400
- NDC
- 54365-400-31
- RECALL-NUMBER
- D-0690-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- unchanged
- created
10. Where is the official source?
Open the official FDA Drug source
Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.