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RecallWatchMedical Device Safety
Class IIOngoingZ-1468-2025

Baxter Healthcare Corporation recalls Progressa Bed Surfaces

Baxter Healthcare CorporationDeerfield, IL, United StatesReported Apr 2, 2025 · 1 year ago
Legal News Analyst ·

Reason for recall

The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.

Lot / code information

UDI
00887761999893; P7520A20S
UDI
00887761999886; P7520A21
UDI
00887761999879; P7520A22S
UDI
00887761999862; P7520A23
UDI
00887761999855; P7520A24S
UDI
00887761999848; P7520A3
UDI
00887761999770; P7520A31
UDI
00887761999756; P7520A37
UDI
00887761999718; P7520A39
UDI
00887761999701; P7520A45
Show 3 more code fields
UDI
00887761999671; P7520A4S
UDI
00887761999657
Serial #
A008MW1489 Y298MW1411 Y298MW1412 Y298MW1413 Y298MW1414 Y298MW1415 Y298MW1416 Y298MW1417 Y298MW1418 Y298MW1419 Y298MW1420 Y298MW1421 Y298MW1452 Y298MW1453 Y298MW1454 Y298MW1455 Y298MW1456 Y298MW1457 Y2…Show all
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What the firm is doing

An URGENT MEDICAL DEVICE CORRECTION notification letter dated 2/25/25 was sent to customers. Actions to be Taken by Customers 1. Please locate all affected units within your facility by reviewing the product label at the head end of the Progressa bed surface with the affected product details provided above. Baxter recommends identifying patients at a higher risk for pressure injuries and placing these patients on alternate beds, if available. 2. A Baxter representative will contact your facility to schedule the correction of your impacted surfaces, or you may contact the Baxter Technical Support Team at 800-445-3720, option 2, between the hours of 8:00 am and 6:00 pm Eastern Time, Monday through Friday. Please work with your Baxter representative to ensure that the affected beds are available for correction (not in use). 3. If you received this communication directly from Baxter, acknowledge receipt by following the instructions on the enclosed reply form instruction sheet, even if you have no remaining inventory. Acknowledging receipt of this notification will prevent you from receiving repeat notices. If you do not complete the acknowledgement, you will receive a phone call from OnProcess Technology on behalf of Baxter to confirm your receipt of this notification. 4. If you purchased this product from a distributor or wholesaler, please note that responding on the Baxter customer portal is not applicable. If a response is requested by your distributor or wholesaler, please respond to them according to their instructions. 5. Please forward a copy of this communication to the Biomedical Engineering Department, and any other departments within your institution who use the affected product. 6. If you are a dealer, wholesaler, distributor/reseller, or original equipment manufacturer (OEM) that distributed any affected product to other facilities, please notify your customers of this Urgent Medical Device Correction in accordance with your customary procedures and ch

DistributionShow details

US Nationwide. Global Distribution.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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