The Recall Desk
Agency classClass IOur severity:SevereFDA (Devices)·Z-1015-2026·Announced 2026-01-28

Red lentil dal soup recalled over undeclared milk and wrong contents

Bakkavor is recalling 291 cases of H-E-B Meal Simple Red Lentil Dal Soup over undeclared milk, with the record citing the wrong product in the container.

The agency’s classification

FDA (Devices): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classified this recall as Class I — a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. On that classification alone this is scored Severe; a score of Critical is reserved for recalls where a death or serious injury was reported. The agency gives the reason as: "Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed…"

Plain-English summary

Meal Simple Red Lentil Dal Soup, net weight 16 oz (1 lb) 454g, under UPC 1 97870 07333 0, made for H-E-B of San Antonio, Texas, is being recalled by Bakkavor.

The reason given in the enforcement record is undeclared milk, with the record stating the wrong product was in the container.

The record lists 291 cases of 6 x 1 lb cups from lot 882428, with a best-by date of 1/11/2026. The record states all product was shipped to one distribution center in Texas. The FDA has classified the action as Class II.

People with a milk allergy can have a reaction after eating a product containing milk when the label does not declare it. Consumers who have this product should not eat it and should follow the retailer's return instructions.

The recalled product

Product
MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
Affected units
35,694

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 (2)

  • UDI/DI 40080196294344
  • All lots

Distribution

Distributed in 4 states:

Part of a larger recall action

This product is one of 6 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →

Similar recalls