Ultra Seal Corporation recalls
Every recall we track for Ultra Seal Corporation — 66 in all, from 2020–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Ultra Seal Corporation peaked in 2022 (56); 66 since 2017.
All FDA recall records for Ultra Seal Corporation 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 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 1 | 2 |
| 2021 | 0 | 0 | 7 | 1 | 8 |
| 2022 | 0 | 0 | 6 | 50 | 56 |
| 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 Ultra Seal Corporation recalls
What to do if you have a recalled Ultra Seal Corporation 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 Ultra Seal Corporation recalls
3 shown- UnratedDrug
Ultra Seal Corporation recalls Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets,
Ultra Seal Corporation recalls 887,000 packets of Pain & Sinus Reliever due to current Good Manufacturing Practice deviations. Check your lot number.
Ultra Seal CorporationJan 24, 2022 - Lower riskDrug
Ultra Seal Corporation recalls Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets Per Packet,
Ultra Seal Corporation recalls Advance Formula Pain Reliever tablets due to unstable salicylic acid levels. Affected lots have specific expiration dates and packaging details. Consumers should check their product labels for the lot numbers and expiration dates listed.
Ultra Seal CorporationOct 13, 2021 - UnratedDrug
Ultra Seal Corporation recalls Pain Relief Maximum Strength (Acetaminophen 250 mg/aspirin 250 mg/Caffeine 65 mg) tablets, 2-tablets per packet,
Ultra Seal recalls Pain Relief Maximum Strength tablets due to failed stability specifications for salicylic acid. Check lot numbers AK8745, AK9751, and AK9552.
Ultra SealAug 3, 2020
Ultra Seal Corporation recall questions
How many recalls has Ultra Seal Corporation had?
66 recalls from Ultra Seal Corporation are on record with U.S. safety agencies, from 2020–2022.
What is the most recent Ultra Seal Corporation recall?
Ultra Seal Corporation recalls Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets,, dated Jan 24, 2022. Every Ultra Seal Corporation recall is listed on this page, newest first.
Why are Ultra Seal Corporation products recalled?
The most common reasons on record: cGMP deviations (56).
What should I do if I have a recalled Ultra Seal Corporation 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 Ultra Seal Corporation 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.