Drug recall
Peng/proc/strep/chlor/hyos (penicillin G, procaine, streptomycin sulfate, chlorpheniramine maleate…
FDA recall event 69442 · Class II · Martin Avenue Pharmacy, Inc.
Key facts
| Event ID | 69442 |
|---|---|
| Recall numbers | V-169-2015, V-170-2015, V-171-2015, V-172-2015, V-173-2015 |
| Recalling firm | Martin Avenue Pharmacy, Inc. |
| Product type | Veterinary |
| Products | Peng/proc/strep/chlor/hyos (penicillin G, procaine, streptomycin sulfate, chlorpheniramine maleate, hyoscyamine sulfate) (vet) injection suspension packaged in an amber glass injectable vial with…, Phenylephrine 1% injectable packaged in an amber glass injectable vial with silver crimp top and sold under the Martin Avenue Pharmacy brand., Prednisolone acetate 50 mg/mL injectable packaged in an amber glass injectable vial with silver crimp top and sold under the Martin Avenue Pharmacy brand., Tacrolimus oil 0.03% opthalmic solution packaged in an opaque squeeze bottle eye dropper, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL., "Tri-mix" 30 mg/3 mg/5 mcg/mL (papaverine, phentolamine mesylate, alprostadil) injectable packaged in a clear glass injectable vial with silver crimp top and sold under the Martin Avenue Pharmacy… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all in-date compounded sterile preparations. The recall is being initiated in connection with a recent FDA inspection due to… |
| Initiation date | Sep 2, 2014 |
| Report date | Nov 12, 2014 |
| Termination date | May 31, 2018 |
| City | Naperville |
| State | IL |
| Country | United States |
| FEI number | 3003381432 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: