Johnson & Johnson Consumer, Inc. recalls
Every recall we track for Johnson & Johnson Consumer, Inc. — 26 in all, from 2017–2021 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Johnson & Johnson Consumer, Inc. peaked in 2021 (20); 26 since 2017. 8% rated “stop using now”.
All FDA recall records for Johnson & Johnson Consumer, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 6 | 0 | 6 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 2 | 0 | 10 | 8 | 20 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Johnson & Johnson Consumer, Inc. recalls
What to do if you have a recalled Johnson & Johnson Consumer, Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Johnson & Johnson Consumer, Inc. recalls
2 shown- UnratedDrug
Johnson & Johnson Consumer, Inc. recalls Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%),
Neutrogena Invisible Daily Defense body spray sunscreen with SPF 60+ is recalled due to cGMP deviations. Affected units may have quality issues affecting safety.
NeutrogenaJul 14, 2021 - Lower riskMedical device
Johnson & Johnson Consumer, Inc. recalls COACH¿ Self-Adhering Sports Wrap (size: 2in)
Johnson & Johnson recalls select COACH Self-Adhering Sports Wraps due to potential natural latex allergy from early manufacturing. Affected products may cause allergic reactions in sensitive individuals.
COACHDec 18, 2017
Johnson & Johnson Consumer, Inc. recall questions
How many recalls has Johnson & Johnson Consumer, Inc. had?
26 recalls from Johnson & Johnson Consumer, Inc. are on record with U.S. safety agencies, from 2017–2021 (20 drug, 6 medical device).
What is the most recent Johnson & Johnson Consumer, Inc. recall?
Johnson & Johnson Consumer, Inc. recalls Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%),, dated Jul 14, 2021. Every Johnson & Johnson Consumer, Inc. recall is listed on this page, newest first.
Why are Johnson & Johnson Consumer, Inc. products recalled?
The most common reasons on record: cGMP Deviations (18); Chemical Contamination: presence of benzene (2).
What should I do if I have a recalled Johnson & Johnson Consumer, Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Johnson & Johnson Consumer, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.