FDA recall record

Med Shop Total Care MORPHINE-BUPIVACAINE-KETAMINE PF INJECTABLE 21 mL syringe in two recall — FDA D-0713-2021

Non-Sterility

Class Iclassification
D-0713-2021official record ID
Aug 18, 2021report date

Recall record at a glance

Official recordD-0713-2021
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMed Shop Total Care Inc.
Report dateAug 18, 2021
Recall initiation dateOct 5, 2020
Quantity21 mL
LocationLongview, TX, United States

Official product description

MORPHINE-BUPIVACAINE-KETAMINE PF INJECTABLE 21 mL syringe in two strengths: a) 5MG-25MG-5MG/ML, b) 1MG-2MG-100MCG/ML, Rx only, Med Shop Total Care 470 East Loop 281 Longview, TX 75605

Why the product was recalled

Non-Sterility

Distribution information

Texas and Puerto Rico

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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