Cape Drugs recalls Methylcobalamin 12mg/ml 1mL vials (Rx only) due to lack of processing controls. Affected lots: 188008, BUD 03/19/2022. No remedy specified in official notice.
Lack of Processing Controls
Cape Drugs is recalling Methylcobalamin 12mg/ml injection vials (1 mL, prescription only) because of processing control issues. This recall affects patients using the medication as prescribed by a doctor. The specific lot number and expiration date are listed in the recall notice.
The recall is due to a lack of processing controls, which could lead to potential quality issues in the medication. However, the official notice does not specify the exact hazard mechanism or how it could cause harm.
Prescription patients using Methylcobalamin 12mg/ml injection vials from Cape Drugs in Annapolis, MD. Patients with the specific lot number 188008 (BUD 03/19/2022) are most at risk.
Check for Methylcobalamin 12mg/ml 1mL vials with lot number 188008, manufactured until 03/19/2022. These vials are sold by Cape Drugs at 1384 Cape St. Claire Road, Annapolis, MD.
Identify the lot number and expiration date on the vial label to confirm if it matches 188008 with BUD 03/19/2022.
The official recall notice does not specify if the medication is safe to use; it only states a lack of processing controls.
The official recall notice does not provide a remedy or action steps for affected products.
Check the lot number on the vial label; affected products have lot number 188008 with an expiration date of 03/19/2022.
We’ve drafted a message you can send Cape Drugs to request your refund or repair — edit it as you like.
Subject: Recall D-0283-2022 — Cape Drugs Cape Drugs Hello, I own a Cape Drugs that is covered by recall D-0283-2022 from Cape Drugs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.