XymoZyme (Health Wright) – Chloramphenicol Contamination (2013)
Class II: 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
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
XymoZyme, dietary supplement, packaged 60 capsules per bottte, 120 capsules per bottle, sold under brand ZYMOGEN.
Brand
Health Wright Products Inc
Lot Codes / Batch Numbers
60 count bottle: LOT# 1207301D, EXP 03/14 (means March 2014), LOT# 1221501D, EXP 08/14 (means August 2014), LOT# 1229205D, EXP 10/14 (means October 2014), 120 count bottle: LOT# 1207301H, EXP 03/14 (means March 2014), LOT# 1221501H, EXP 08/14 (means August 2014), LOT# 1229205H, EXP 10/14 (means October 2014)
Products Sold
60 count bottle: LOT# 1207301D, EXP 03/14 (means March 2014); LOT# 1221501D, EXP 08/14 (means August 2014); LOT# 1229205D, EXP 10/14 (means October 2014); 120 count bottle: LOT# 1207301H; EXP 03/14 (means March 2014); LOT# 1221501H, EXP 08/14 (means August 2014); LOT# 1229205H, EXP 10/14 (means October 2014);
Health Wright Products Inc is recalling XymoZyme, dietary supplement, packaged 60 capsules per bottte, 120 capsules per bottle, sold under due to Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, OR, UT
Page updated: Jan 6, 2026