The Recall Desk
SevereFDA (Drugs)·D-0755-2019·Announced 2019-03-20

King Bio Recalls Dr. King's SafeCare Rx Bone Strengthener Due to Microbial Contamination

King Bio Inc. is recalling 244 bottles of Dr. King's SafeCare Rx Bone Strengthener due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that use of the product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a severity score of 4 or higher.

Plain-English summary

King Bio Inc. is recalling 244 bottles of Dr. King's SafeCare Rx Bone Strengthener, 2 fl. oz. (59 mL), due to microbial contamination. The product is identified by NDC 57955-0070-2 and UPC 357955007029.

The recalled lots include 060316F (Exp. 06/19), 022316B (Exp. 02/19), and 122216H (Exp. 12/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers should check their inventory for these specific lot numbers and expiration dates. If they possess the recalled product, they should stop using it and contact King Bio Inc. for further instructions.

The recalled product

Product
Dr. King's SafeCare Rx Bone Strengthener, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007029, NDC 57955-0070-2
Manufacturer
King Bio Inc.
Affected units
244

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lots: 060316F Exp. 06/19
  • 022316B Exp. 02/19
  • 122216H Exp. 12/19

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 465 recalled by King Bio Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 465 products in this recall →