Use caution Drug recall · FDA · Published November 11, 2015

Bicillin L-A Recall: Incorrect Storage Instructions

RemedyRepack Inc. recalls Bicillin L-A syringes due to incorrect storage instructions on the label. Check lot numbers and expiration dates.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0512-2016Drug Bicillin ›

Use caution until it’s fixed

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Take action

Contact the company

Recalling firmRemedyRepack Inc.625 Kolter Dr Ste 4 · Indiana, PA 15701-3571

✎ GovInfoNow plain-language explainer

RemedyRepack Inc. is recalling specific lots of Bicillin L-A injection syringes because the labeling contains incorrect storage instructions. The product was manufactured by King Pharma Inc. and distributed nationwide. No other hazards or injuries are mentioned in this record. Read more at govinfonow.com/recall/43357-remedyrepack-inc-recalls-bicillin-l-a-600000-units-ml-inj.

Source Summary by GovInfoNow · govinfonow.com/recall/43357-remedyrepack-inc-recalls-bicillin-l-a-600000-units-ml-inj · Updated October 11, 2026 · FDA enforcement record: FDA #D-0512-2016

Cite this page

“Bicillin L-A Recall: Incorrect Storage Instructions.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43357-remedyrepack-inc-recalls-bicillin-l-a-600000-units-ml-inj. Based on FDA recall #D-0512-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0512-2016%22&limit=1).

The FDA announced on 2015-11-11 that RemedyRepack Inc. is recalling Bicillin L-A Injection Syringes due to incorrect storage instructions on the label. The recall affects 60 vials distributed nationwide.

How to tell if you have it

Brand: Bicillin
Product: Bicillin L-A Injection Syringe
Quantity: 20 mL Syringe
Manufacturer: King Pharma Inc., Bristol, TN 37620
Repackager: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701
NDC: 61786-0253-03
Lot Codes: B0077329-040215 (Exp 07/2017), B0091342-070315 (Exp 08/2017), B0109416-102815 (Exp 03/2018)
Distribution: Nationwide

The hazard

The recall is due to incorrect storage instructions on the product labeling. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show RemedyRePack Inc. has 35 other recalls on record since 2015-02-18. Other recent recalls of similar products include American Regent Levocarnitine Injection Recall (2026-04-16), American Health Packaging Buprenorphine Tablets Recall (2026-08-19), and McKesson Gemcitabine Injection Recall (2026-06-10).

How to tell if you have this one

Look for Bicillin L-A 600000 Units/mL Inj. in a 20 mL Syringe. Check for NDC 61786-0253-03 and one of the following lot numbers: B0077329-040215 (Exp 07/2017), B0091342-070315 (Exp 08/2017), or B0109416-102815 (Exp 03/2018).

Brand
Bicillin
Category
Drug

FDA recall event · 7 products

All 7 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
Nationwide

Recall number	Product, codes & lots	Quantity
D-0511-2016	Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08; LOT # B0080702-042715, B0080695-042715, B0097444-082015, Exp 07/2017; B0097443-082015, Exp 02/2018.	65 Vials
D-0512-2016	Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03; Lot # B0077329-040215, Exp 07/2017; B0091342-070315, Exp 08/2017; B0109416-102815, Exp 03/2018	60 Vials
D-0513-2016	Vitamin B-Complex 100, Multi MG Inj, Qty: 30 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0873-02; Lot # B0105037-100715, Exp 10/01/2016	1 Vial
D-0514-2016	Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16; LOT # B0105052-100715, Exp 07/01/2017	1 Vial
D-0515-2016	Lorazepam 2 mg/mL Inj., Qty: 1 mL Vial, MFG by: West-Ward Pharma, Eatontown, NJ 07724, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0316-01; LOT#: B0085124-051915, B0086919-052815, Exp 12/01/2016; B0089280-061215, B0090023-061915, B0089996-061915, B0091581-070715, B0091564-070715, B0091515-070715, Exp 01/01/2017; B0094980-080415, B0094965-080415, B0097515-082415, B0100639-091415, B0100611-091415, Exp 03/01/2017; B0100933-091515, B0107165-101915, B0107118-101915, Exp 06/01/2017.	1625 Vials
D-0516-2016	Novolin 70/30, 100 Units/mL Solu., Qty: 1 Vial, MFG by: Novo Nordisk, A/S, Bagsvaerd, Denmark DK-2880, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0414-01; LOT#:QM114CZF0496, Exp 01/2016; B0025373-050514, B0029738-060914, Exp 02/2016; B0029737-060914, Exp 03/2016.	106 Vials
D-0517-2016	Rocuronium Bromide 50 MG/5ML INJ., Qty: 5 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0222-57; Lot#: B0073852-030915, Exp 04/2016	4 Vials

Based on the official FDA remedy

What to do — step by step

Check Your Product Details
Verify if your syringe matches the NDC and lot numbers listed in the recall record.
Contact RemedyRepack Inc.
The record does not specify a remedy or return process, so you should contact the manufacturer directly for further instructions.

Where it went and when

Where it was distributed

Distributed nationwide.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

Nov 11, 2015Firm started the recall
Dec 4, 2015FDA classified it Class II
Dec 16, 2015Published in FDA’s Enforcement Report
Nov 1, 2016FDA terminated the recall

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

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Keep exploring

Link to this recall

<a href="https://govinfonow.com/recall/43357-remedyrepack-inc-recalls-bicillin-l-a-600000-units-ml-inj">Bicillin L-A Recall: Incorrect Storage Instructions (GovInfoNow)</a>

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-0512-2016 (November 11, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0512-2016 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.