CLASS II Drug recall · Reported 21 Aug 2019 · FDA Enforcement Report
Cryo-273 Cold Pain Relieving Gel recalled by US Pharmaceuticals
US Pharmaceuticals is recalling Cryo-273 Cold Pain Relieving Gel, distributed nationwide in the US. The recall was initiated on 11 Jul 2019 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1741-2019
- FDA event ID
- 83316
- Recalling firm
- US Pharmaceuticals, Belleville, NJ
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 11 Jul 2019
- FDA classified
- 13 Aug 2019
- Reported
- 21 Aug 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Potency & Assay
- Drug class
- Creams, Ointments & Gels
Timeline
| 11 Jul 2019 | Recall initiated by company | |
| 13 Aug 2019 | Classified by FDA | +33 days |
| 21 Aug 2019 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.
Product as listed by the FDA
CRYO-273 Cold Pain Relieving Gel 128 FL. OZ. Distributed By: CRYO-273.com Tampa, FL 33629. UPC 8 15290 01550 2
Where it was distributed
Distributed Nationwide in the USA
Questions about this recall
Why was it recalled?
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Which lots are affected?
Lot #'s 13K17 EXP 08/2019, 03L17 EXP 09/2019, 74H18 EXP 06/2020, 18J18 EXP 06/2020
Where was it sold?
Distributed Nationwide in the USA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
17 other products · FDA event 83316More recalls from US Pharmaceuticals
All 22| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | CVS Health Hydrating Healing Ointment (Petrolatum 41%) recalled | US Pharmaceuticals | Manufacturing (CGMP) Deviations | RI |
| Drug | CLASS II | Children Glycerin Suppositories Laxative for ages 2 to Package Size recalled | US Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | CVS Health Glycerin Suppositories recalled by US Pharmaceuticals | US Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Adult Glycerin Suppositories, Package Size suppositories recalledWalgreens Adult Glycerin | US Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | CVS Therapeutic Menthol Gel recalled by US Pharmaceuticals | US Pharmaceuticals | Potency & Assay | Nationwide |