Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported July 1, 2020
R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 mL in 60 mL Syringe, Compounded by QuVa 519 Bloombury, NJ 08804, NDC 70092143350
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
QuVa Pharma, Inc. recalled R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 … - a low-severity action.
R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 … was recalled by QuVa Pharma, Inc. in July 1, 2020. Reason: Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac. Check the official notice for the remedy. Verify recall #D-1335-2020 with the FDA Drug before acting.
The recall
QuVa Pharma, Inc. issued this low-severity FDA Drug recall-Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac.
- Low
- severity level
- Class III
- classification
- July 1, 2020
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1335-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1335-2020) was formally reported on July 1, 2020, with the manufacturer initiating the action on April 23, 2020. It is classified under Low severity (Class III), with a current status of Terminated. QuVa Pharma, Inc. is listed as the recalling firm, operating out of Sugar Land, TX. Federal records list the affected scope as 17,050 syringes.
The documented reason for this recall is: Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac Distribution data in the federal record shows the product reached: Distributed Nationwide in the US.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
17,050 syringes
Related Recalls
6
0 from same agency
Product description
R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 mL in 60 mL Syringe, Compounded by QuVa 519 Bloombury, NJ 08804, NDC 70092143350
Reason for recall
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1335-2020 |
| Date reported | July 1, 2020 |
| Date initiated | April 23, 2020 |
| Recalling firm | QuVa Pharma, Inc. |
| Firm location | Sugar Land, TX |
| Affected scope | 17,050 syringes |
| Distribution | Distributed Nationwide in the US. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-1335-2020) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 mL in 60 mL Syringe, Compounded by QuVa 519 Bloombury, NJ 08804, NDC 70092143350. Recalled by QuVa Pharma, Inc.. Units affected: 17,050 syringes.
Why was this product recalled? ▼
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 1, 2020. Severity: Low. Recall number: D-1335-2020.
Where was the recalled product distributed? ▼
Distribution: Distributed Nationwide in the US..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1335-2020) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported July 1, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.