FDAClass IINovember 4, 2020

CMEAmerica BodyGuard Wall Charger recall

CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X L0/$$72019-0364/ 16D20191101/* Lot Number…

Why was CMEAmerica BodyGuard Wall Charger recalled?

The wall charger may not properly charge the infusion pump battery.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Catalog NO. 151-143XL LOT NO. 2019-0364

Product
CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X L0/$$72019-0364/ 16D20191101/* Lot Number…
Recalling firm
CME America LLC
Quantity
27 chargers
Distribution
U.S. Consignees: 3, IL, MO, KS OUS : 0 "No foreign consignees".
Recall date
November 4, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls