Food, drugs, devices › West-Ward Pharmaceutical Corp.

Drug recall: Carisoprodol Tablets, USP 350 mg, Rx Only, 1000 tablets. Dist by: West-ward Pharmaceutical Corp. Eatontown, NJ 07724. Mf

FDA enforcement event 67022 · Class II · initiated 7 Nov 2013 · status Terminated · terminated 14 Aug 2014

DrugVoluntary: Firm initiated1 product recordEatontown, NJ

West-Ward Pharmaceutical Corp. (Eatontown, NJ) initiated this drug recall on 7 Nov 2013; FDA lists 1 product record under event 67022, classified Class II.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 56% of the 370 drug enforcement events initiated in 2013 carry the same class.

Status: Terminated, terminated 14 Aug 2014. Initiation: voluntary: firm initiated. West-Ward Pharmaceutical Corp. has 24 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

West-Ward Pharmaceutical Corp., Eatontown, NJ.

Reason for recall

"Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine stability testing"

Distribution

"Nationwide"

Product records

Recall number	Product	Quantity	Class	Status	Report date
D-367-2014	Carisoprodol Tablets, USP 350 mg, Rx Only, 1000 tablets. Dist by: West-ward Pharmaceutical Corp. Eatontown, NJ 07724. Mfd by: Shasun Chemicals and Drugs Limited, Unit II, R. S. Na 32, 33, 743 PIMS Rd, Periyakalepet, Pondicherry. 605014 INDIA. NDC 0143-9749-10.	20,534 bottles	Class II	Terminated	25 Dec 2013

Context

56%of 2013 drug events are Class II370 events that year

1product record in this eventfirm median: 1

24events on this register for the firm

Other enforcement events for West-Ward Pharmaceutical Corp.

Initiated	Product (first record)	Type	Class	Records
13 May 2015	Fentanyl Citrate Inj., USP, CII, 250 mcg/5 mL (50 mcg/mL) (0.05 mg/mL), Rx Only, For IV or IM Use Preservative Free, 25	Drug	Class III	1
2 Oct 2014	VERSAPHARM INCORPORATED Ethambutol Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx Only, Manufactured for Versa	Drug	Class II	1
20 May 2014	Isoniazid Tablets, USP, 300 mg, Rx only, packaged in a) 100-count bottles, NDC 0143-1261-01, b) 1000-count bottles, NDC	Drug	Class II	1
23 Sep 2013	Irinotecan Hydrochloride Injection, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial per carton, Rx only, Manufactured b	Drug	Class II	2
30 Jul 2013	Lisinopril Tablets, USP, 2.5 mg, Rx only, packaged in a) 100-count bottles (NDC 0143-1265-01) and b) 1000-count bottles	Drug	Class II	1
30 Jul 2013	Belladonna Alkaloids with Phenobarbital Tablets, 1000 count (NDC 0143-1140-10) and 5000 count (NDC 0143-1140-51) PET bot	Drug	Class II	1
4 Jun 2013	VersaPharm Incorporated, Ethambutol Hydrochloride Tablets, USP 400 mg 60 tablets, Rx Only, Mfd. for VersaPharm Incorpora	Drug	Class II	1
16 May 2013	West-ward Belladonna Alkaloids with Phenobarbital Tablets, a) 1000-count bottle (NDC 0143-1140-10), b) 5000-count bottle	Drug	Class II	2
13 May 2013	Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL), 10 mL single-use vials, Rx Only, Mfd. by Exela Pharma Scien	Drug	Class III	1
18 Mar 2013	Ethambutol Hydrochloride Tablets, USP, 100 mg, 100-count tablets per bottle, Rx only, Mfd. for: Versapharm Incorporated,	Drug	Class II	1

All 24 events for West-Ward Pharmaceutical Corp.

Questions and answers

Why was this drug recalled?

FDA's record gives the reason for recall as: "Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine stability testing"

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "Nationwide"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 14 Aug 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA drug enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.