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Unrated Drug recall · FDA · Published December 3, 2021

Cape Drugs B-Complex Injections Recall: Lack of Processing Controls

Cape Drugs recalls B-Complex injections due to lack of processing controls. Affected lots were sold at Cape Drugs locations in Annapolis, MD. Consumers should check product labels for lot number 190036.

🇺🇸 FDA recall #D-0284-2022DrugCape Drugs ›
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Contact the company

Recalling firmValgene Incorporated dba Cape Drugs1384 Cape St Claire Rd · Annapolis, MD 21409-5325
✎ GovInfoNow plain-language explainer

Cape Drugs is recalling B-Complex injection vials (1 mL, prescription only) because of a lack of processing controls. This could lead to potential quality issues with the medication. Consumers should check their product labels for the specific lot number. Read more at govinfonow.com/recall/35495-cape-drugs-b-complex-injections-recall-lack-of-processing-controls.

Source Summary by GovInfoNow · govinfonow.com/recall/35495-cape-drugs-b-complex-injections-recall-lack-of-processing-controls · Updated September 23, 2026 · FDA enforcement record: FDA #D-0284-2022

Cite this page

“Cape Drugs B-Complex Injections Recall: Lack of Processing Controls.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/35495-cape-drugs-b-complex-injections-recall-lack-of-processing-controls. Based on FDA recall #D-0284-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0284-2022%22&limit=1).

Valgene Incorporated dba Cape Drugs recalled B-Complex injection vials on Dec. 3, 2021, due to a lack of processing controls, the FDA said. The recall was voluntary and classified as Class II.

How to tell if you have it

  • Brand: Cape Drugs
  • Product: B-Complex, injection, 1 mL vials
  • Lot#: 190036
  • BUD: 12/27/2021
  • Quantity: 12 vials
  • Distribution: Maryland Only

The hazard

The recall was issued because of a lack of processing controls for the B-Complex injection vials, according to the FDA.

Context

GovInfoNow's records show other recent recalls of similar products include Baxter Clindamycin Injection Recall (2026-08-06), Baxter Healthcare Daptomycin Injection Recall (2026-08-06) and Baxter Famotidine Injection Recall (2026-08-06).

How to tell if you have this one

Check the product label for the lot number 190036 and the expiration date of December 27, 2021. The product was sold at Cape Drugs locations in Annapolis, MD.

  • Brand
    Cape Drugs
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Maryland Only
Recall numberProduct, codes & lotsQuantity
D-0283-2022Methylcobalamin 12mg/ml injection, 1 mL vials, Rx only, Cape Drugs 1384 Cape St. Claire Road Annapolis, MD 21409; Lot #: 188008, BUD 03/19/202227 vials
D-0284-2022B-Complex, injection, 1 mL vials, Rx only, Cape Drugs 1384 Cape St. Claire Road Annapolis, MD 21409; Lot# 190036, BUD 12/27/202112 vials
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number 190036 and expiration date of December 27, 2021 on the vial.

Where it went and when

Where it was distributed

Distributed in Maryland.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Maryland Only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland.

Recall timeline

FDA terminated this recall 32 days after the firm started it.

1. Firm started the recall: Dec 3, 202112. FDA classified it Class II: Dec 15, 202123. Published in FDA’s Enforcement Report: Dec 22, 202134. FDA terminated the recall: Jan 4, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0284-2022 (December 3, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0284-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA