Johnson & Johnson Consumer, Inc.
Johnson & Johnson Consumer, Inc. holds FDA 510(k) medical device clearances, cleared in 2018, with 6 FDA device recalls on record.
Top product codes for Johnson & Johnson Consumer, Inc.
FDA recalls by Johnson & Johnson Consumer, Inc.
- Z-1204-2018 — Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 3in)
- Z-1201-2018 — COACH¿ Self-Adhering Sports Wrap (size: 2in)
- Z-1206-2018 — Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 2in)
- Z-1205-2018 — Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 1in)
- Z-1203-2018 — Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 2in)
- Z-1202-2018 — COACH¿ Self-Adhering Sports Wrap (size: 3in)
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Johnson & Johnson Consumer, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.